Pet food and pet product recalls
1057 federal recalls on file. Federal recalls for dog and cat food, treats, chews, supplements, and pet products. Sourced from the FDA and USDA and translated into plain English.
- 2026-05-06FDA-PRStop feeding Albright's Raw Pet Food chicken recipe
Albright’s Raw Pet Food of Fort Wayne, Indiana out of an abundance of caution is voluntarily recalling one lot of its Chicken Recipe for Dogs Complete and Balanced because this lot has the potential to be contaminated with Salmonella.
- 2026-05-05FDA-PRWinfield’s Chocolate BarDiscard Winfield's dark chocolate bars if you have milk allergy
HOUSTON, TX, May 5, 2026 — CBSL Commissary LLC, operating as Winfield’s Chocolate Bar, is voluntarily recalling five dark chocolate products sold at its three Houston, Texas locations because the word “milk” was omitted from the ingredient label. Milk is a known major food allergen under the Food Al
- 2026-04-30CPSCCBC Group, Inc., of Phoenix, ArizonaStop using Stephan Baby toy cubes immediately
The toys' plastic cube can break into small parts or sharp edges, posing a risk of serious injury from choking and laceration hazards.
- 2026-04-23CPSCShenzhen Leye E-commerce Co., Ltd., dba MISSJUNE, of ChinaStop using KMUYSL Big Red Barn toy set
The recalled children's toys violate the small parts ban because the toy is intended for children under three years of age and the fence handles can detach from the toy, posing a deadly choking hazard.
- 2026-04-23CPSCLander Enterprises LLC, dba Autobrush, of Miami, FloridaStop using Autobrush Sonic Pro toothbrush boxes
The recalled delivery boxes violate the mandatory standard for consumer products containing button cell and coin batteries because they contain a lithium coin battery that can be easily accessed by children, posing an ingestion hazard. The packaging also does not bear the required warning labels for products containing such batteries as required by Reese's Law. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns, and death.
- 2026-04-17FDA-PRRevival Animal Health, LLCStop feeding Revival canine milk replacers
Revival Animal Health of Orange City, IA is recalling Breeder’s Edge® Foster Care® Canine and Shelter’s Choice® Canine Milk Replacers due to variable levels of Vitamin D resulting in both low and elevated levels in some of the canine milk replacers.
- 2026-04-16CPSCShims Bargain, Inc., dba JC Sales, of Los Angeles, CaliforniaStop using JC Sales Lil' Buddies Pet Laser Toys
The Montessori toy sets contain an airplane shaped teething toy that has tentacle ends that can pose a choking hazard to young children. The toys also violate the teething toy provision of the mandatory standard for children's toys.
- 2026-04-16CPSCShen Zhen Zhuoyuechaoqun Electronic Commerce Co., Ltd., dba Melofaver US, of ChinaStop using ATOYUS activity cube toy
The recalled toys violate the small parts ban because the toys are intended for children under three and the toys' xylophone screws and clock hands can detach. In addition, the toys violate the mandatory safety standard for children's toys because the mallets have spherical ends, posing a choking hazard.
- 2026-04-16CPSCGuangzhou Letao Keji Youxiangongsi, doing business as Letokids, of ChinaRemove batteries from Sanlebi Pet Vet Playset immediately
The Pet Vet Playset violates the mandatory standard for toys because the button cell batteries in the nail grinder and otoscope can be easily accessed by children.
- 2026-03-19CPSCDongguanshi Aokaolan Trading Co., Ltd., dba Goregent Official Store, of ChinaInfant Walkers Recalled Due to Risk of Serious Injury or Death from Fall Hazard; Violate Mandatory Standard for Infant Walkers; Sold on Amazon by Goregent Official Store
The recalled infant walkers violate the mandatory standard for infant walkers because they can fit through a standard doorway and fail to stop at the edge of a step, posing a risk of serious injury or death due to a fall hazard.
- 2026-02-26CPSCSN Commerce LLC, dba TheKiddoSpaceStore, of Dover, DelawareTheKiddoSpace Recalls Children's Flashcard Talking Toys Due to Risk of Injury from Lead and Phthalate Exposure; Violates Federal Lead Content and Phthalates Bans and Standard for Toys
The recalled children's flashcard toy sets contain levels of lead that exceed the federal lead content ban and levels of phthalates that exceed the federal phthalates ban. Lead and phthalates are toxic if ingested by young children and can cause adverse health issues. In addition, the flashcards also violate the mandatory standard for toys because they fail to comply with the short circuit protection requirement for battery-operated toys.
- 2026-02-26CPSCSN Commerce LLC, dba TheKiddoSpaceStore, of Dover, DelawareTheKiddoSpace Recalls Children's Handwriting Practice Kits Due to Risk of Injury from Lead Exposure; Violates Federal Lead Content Ban
The pens in the recalled children's handwriting kits contain levels of lead in the nib that exceed the federal lead content ban. Lead is toxic if ingested by young children and can cause adverse health issues.
- 2026-02-25FDA-DeviceMedline Industries, LPClass IIMedline Surgical Drapes: 1) SHEET,DRAPE,40X58,STERILE, Model Number: DYNJP2410; 2) DRAPE,SHEET,ECONOMY,40X58",ST,20/CS, Model Number: DYNJP2411; 3) SHEET,DRAPE, 40X70,STERILE, Model Number: DYNJP2412; 4) DRAPE,MEDIUM,TAPE,40X70",ST,50/CS, Model Number: DYNJP2412T; 5) SHEET,DRAPE,53X77,STERILE, Model Number: DYNJP2414; 6) DRAPE,SHEET,3/4,53X77",ST,20/CS, Model Number: DYNJP2414R; 7) DRAPE,SHEET,ULTRAGARD,20/CS, Model Number: DYNJP2414UG; 8) DRAPE,RNF,53X77",ST,20/CS, Model Number:
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
- 2026-02-25FDA-DeviceBard Peripheral Vascular IncClass IIBroviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff Cat 60060
Due to damage to outer tray that can potentially compromise the sterile barrier
- 2026-02-19CPSCMeijer Distribution, Inc., of Grand Rapids, MichiganMeijer Recalls Lullaby Lane and MCS Children's Sleepwear Due to Burn Hazard; Violates Mandatory Standard for Children's Sleepwear
The recalled sleepwear violates the mandatory flammability standard for children's sleepwear, posing a risk of burn injuries to children.
- 2026-02-18FDA-FoodKPCM New York Inc.Class IIa.) Preema brand Bright Red Food Colour Powder; Net Weight .88oz/25gm; packaged in small plastic bottle; INGREDIENTS: SODIUM CHLORIDE, COLOUR (TARTRAZINE, CARMOSINE, ALLURA RED) CHECK THE LEGAL LIMIT, CONTAINS NO ANIMAL MATTER. E102, E122, E129 may have an adverse effect on activity and attention in children b.) Preema brand Orange Food Colour Powder; Net Weight .88oz/25gm; packaged in a small plastic bottle; INGREDIENTS: SODIUM CHLORIDE, COLOUR (TARTRAZINE, CARMOSINE, ALLURA RED) CHECK THE LEG
Products contain banned color, carmoisine and undeclared FD&C Yellow 5 and FD&C Red 40
- 2026-02-11FDA-DeviceFujirebio Diagnostics, Inc.Class IIProduct Name: Lumipulse ¿-Amyloid Plasma Controls Model/Catalog Number: 81559 Software Version: Not Applicable Product Description: Lumipulse ¿-Amyloid Plasma Controls: This quality control product can be used as an objective judgement of the laboratory s procedures and personnel techniques when analyzing ¿-amyloid1-42 in K2EDTA plasma on the LUMIPULSE G System. It is a valuable tool to assess good laboratory practices. Two levels of control are available to compare observations with expecte
Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low specificity when compared back to FDA-cleared CSF ratio/PET imaging, due to falsely elevated positive ratio or falsely elevated indeterminate ratio results causing an incorrect classification of a patient as having amyloid pathology associated with Alzheimer s disease (positive result) and/or requiring more clinical testing of that patient (indeterminate result).
- 2026-02-11FDA-DeviceFujirebio Diagnostics, Inc.Class IIProduct Name: Lumipulse G ¿-Amyloid 1-42-N Plasma Calibrators Model/Catalog Number: 235454 Software Version: Not Applicable Product Description: Lumipulse G ¿-Amyloid 1-42-N Plasma Calibrators: The ¿-Amyloid 1-42 plasma concentration of a specimen is automatically calculated from the calibration curve, which is automatically calculated from calibration data. The result of the calculation is reported in pg/mL. Lumipulse G ¿-Amyloid 1-42-N Plasma Calibrators: Liquid (Frozen), 1 ¿ 1.5 mL (4
Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low specificity when compared back to FDA-cleared CSF ratio/PET imaging, due to falsely elevated positive ratio or falsely elevated indeterminate ratio results causing an incorrect classification of a patient as having amyloid pathology associated with Alzheimer s disease (positive result) and/or requiring more clinical testing of that patient (indeterminate result).
- 2026-02-11FDA-DeviceFujirebio Diagnostics, Inc.Class IIProduct Name: Lumipulse G ¿-Amyloid 1-42-N Plasma Immunoreaction Cartridges Model/Catalog Number: 235447 Software Version: Not Applicable Product Description: Lumipulse G ¿-Amyloid 1-42-N Plasma Immunoreaction Cartridges (IRC): Lumipulse G ¿-Amyloid 1-42-N Plasma is an assay system, including a set of immunoassay reagents (Lumipulse G ¿-Amyloid 1-42-N Plasma IRC), for the quantitative measurement of ¿-Amyloid 1-42 in K2EDTA plasma specimens based on chemiluminescent enzyme immunoassay (CLEI
Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low specificity when compared back to FDA-cleared CSF ratio/PET imaging, due to falsely elevated positive ratio or falsely elevated indeterminate ratio results causing an incorrect classification of a patient as having amyloid pathology associated with Alzheimer s disease (positive result) and/or requiring more clinical testing of that patient (indeterminate result).
- 2026-02-11FDA-DeviceFujirebio Diagnostics, Inc.Class IIProduct Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Product Description: Lumipulse pTau 217 Plasma Controls: This quality control product can be used as an objective judgement of the laboratory s procedures and personnel techniques when analyzing pTau 217 in K2EDTA plasma on the LUMIPULSE G System. It is a valuable tool to assess good laboratory practices. Two levels of control are available to compare observations with expected range
Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low specificity when compared back to FDA-cleared CSF ratio/PET imaging, due to falsely elevated positive ratio or falsely elevated indeterminate ratio results causing an incorrect classification of a patient as having amyloid pathology associated with Alzheimer s disease (positive result) and/or requiring more clinical testing of that patient (indeterminate result).
- 2026-02-11FDA-DeviceFujirebio Diagnostics, Inc.Class IIProduct Name: Lumipulse G pTau 217 Plasma Calibrators Model/Catalog Number: 81557 Software Version: Not Applicable Product Description: Lumipulse G pTau 217 Plasma Calibrators: The pTau 217 plasma concentration of a specimen is automatically calculated from the calibration curve, which is also automatically calculated from calibration data. The result of the calculation is reported in pg/mL. Lumipulse G pTau 217 Plasma Calibrators: Liquid (Frozen), 1x1.5 mL (5 Concentrations) CAL 1
Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low specificity when compared back to FDA-cleared CSF ratio/PET imaging, due to falsely elevated positive ratio or falsely elevated indeterminate ratio results causing an incorrect classification of a patient as having amyloid pathology associated with Alzheimer s disease (positive result) and/or requiring more clinical testing of that patient (indeterminate result).
- 2026-02-11FDA-DeviceFujirebio Diagnostics, Inc.Class IIProduct Name: Lumipulse G pTau 217 Plasma Immunoreaction Cartridges Model/Catalog Number: 81550 Software Version: Not Applicable Product Description: Lumipulse G pTau 217 Plasma Immunoreaction Cartridges (IRC): Lumipulse G pTau 217 Plasma is an assay system, including a set of immunoassay reagents (Lumipulse G pTau 217 Plasma IRC), for the quantitative measurement of pTau 217 in K2EDTA plasma specimens based on chemiluminescent enzyme immunoassay (CLEIA) technology by a specific two-step imm
Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low specificity when compared back to FDA-cleared CSF ratio/PET imaging, due to falsely elevated positive ratio or falsely elevated indeterminate ratio results causing an incorrect classification of a patient as having amyloid pathology associated with Alzheimer s disease (positive result) and/or requiring more clinical testing of that patient (indeterminate result).
- 2026-02-11FDA-DeviceFujirebio Diagnostics, Inc.Class IIProduct Name: Lumipulse G pTau217/B-Amyloid 1-42 Plasma Ratio Model/Catalog Number: CL0073 Software Version: Not Applicable Product Description: Lumipulse G pTau217/¿-Amyloid 1-42 Plasma Ratio is an in vitro diagnostic (IVD) test that combines the test results of the Lumipulse G pTau 217 Plasma assay and the Lumipulse G ¿-Amyloid 1-42-N Plasma assay from the same patient specimen (K2EDTA plasma sample) into a numerical ratio. The Lumipulse G pTau 217/¿-Amyloid 1-42 Plasma Ratio Instructions F
Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low specificity when compared back to FDA-cleared CSF ratio/PET imaging, due to falsely elevated positive ratio or falsely elevated indeterminate ratio results causing an incorrect classification of a patient as having amyloid pathology associated with Alzheimer s disease (positive result) and/or requiring more clinical testing of that patient (indeterminate result).
- 2026-02-11FDA-DeviceVortex Surgical Inc.Class IIVortex Surgical 1. 23GA Laser Probe Curved Cat No. VS0120.23 2. 25GA Laser Probe Curved Cat No. VS0120.25 3. 25GA Laser Probe Flex-Tip Cat No. VS0130.25 4. 25GA Laser Probe Illuminated Curved Cat No. VS0125.25B 5. 25GA Laser Probe MaxReach Cat No. VS0140.25 6. 25GA Laser Probe Straight Cat No. VS0110.25
There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which could lead to infection.
- 2026-01-29CPSCHobby Lobby Stores, Inc. of Oklahoma City, OklahomaHobby Lobby Recalls Giraffe and Llama Plush Toys with Clips Due to Choking Hazard
The legs of the plush toy can detach from the body allowing the release of small beads that are on the legs, posing a choking hazard to young children.
- 2026-01-28FDA-DeviceGE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGINGClass IIGE Healthcare Omni Legend, sold under the following names: OMNI Legend 16, Omni Legend 21, OMNI Legend 32, Omni Legend PET Gantry 16cm - MEA, Omni Legend PET Gantry 16cm Haifa LM, Omni Legend PET Gantry 16cm Mobile, Omni Legend PET Gantry 21cm - BJ for Global, Omni Legend PET Gantry 21cm - Global Haifa LM, Omni Legend PET Gantry 21cm - Mobile, Omni Legend PET Gantry 21cm WSO LM, Omni Legend PET Gantry 32cm - MEA, Omni Legend PET Gantry 32cm Haifa LM, Omni Legend PET Gantry 32cm Mobile, OMNI
There is a potential intermittent issue on certain Omni Legend systems that can result in a streaking artifact in the PET clinical scan images. This streaking artifact is most easily identified in transaxial slices on the acquisition console (both corrected and non-corrected for attenuation).
- 2026-01-08CPSCSarnia Sales LLC, dba Joyful Journeys, of Issaquah, WashingtonJoyful Journeys Recalls Baby Loungers Due to Risk of Serious Injury or Death from Entrapment and Fall Hazards; Violates Mandatory Standard for Infant Sleep Products
The recalled baby loungers violate the mandatory safety standard for Infant Sleep Products. The sides are too low to contain an infant and the enclosed openings at the foot of the loungers are wider than allowed, posing serious risks of fall and entrapment hazards to infants. In addition, the baby loungers do not have a stand, posing a fall hazard if used on elevated surfaces. These violations create an unsafe sleeping environment and can cause death or serious injury to infants.
- 2025-12-24FDA-DeviceCopan ItaliaClass II1ml of DTT in liquid phase, in PET tube with capture cap, in bulk
Treatment reagent functionality in respiratory specimens fluidification cannot be guaranteed.
- 2025-12-24FDA-DeviceCopan ItaliaClass II1ml of DTT in liquid phase, in PET tube with capture cap, in bulk + sputum transfer device, for WASP* *Compatible with Copan s WASP (Walk-Away Specimen Processor for Microbiology) System
Treatment reagent functionality in respiratory specimens liquification cannot be guaranteed.
- 2025-12-10FDA-DeviceGET TESTED INTERNATIONAL ABClass IIPet Allergy Test
Distribution without premarket approval/clearance.
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