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Search every CPSC, FDA, USDA and NHTSA recall on record, or scan a barcode. The last 90 days are below.
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Stop using Stephan Baby toy cubes immediatelyThe water-filled plastic cubes in Stephan Baby Boo Bunnie and Friends plush toys can crack or break into small sharp pieces. One child swallowed sharp pieces from a broken cube. About 227,500 toys sold since August 2017 are affected.
SeriousCPSCApr 30, 2026
Stop using KMUYSL Big Red Barn toy setThe fence handles on this toy barn set can detach and pose a serious choking risk to young children. The toy is marketed for children under 3 years old but contains small parts that violate federal safety rules. About 3,000 sets sold on Amazon between July 2023 and June 2025.
SeriousCPSCApr 23, 2026
Stop using Autobrush Sonic Pro toothbrush boxesAutobrush Sonic Pro Kids toothbrush delivery boxes contain a coin cell battery that children can easily access and swallow. Swallowing these batteries can cause serious internal burns or death. The packaging also lacks required warning labels.
SeriousCPSCApr 23, 2026
Stop feeding Revival canine milk replacersRevival Animal Health is recalling Breeder's Edge® Foster Care® and Shelter's Choice® Canine Milk Replacers because some batches contain unsafe vitamin D levels—either too low or too high. Dogs eating products with high vitamin D may develop serious health problems including kidney disease.
SeriousFDAApr 17, 2026
Stop using JC Sales Lil' Buddies Pet Laser ToysJC Sales recalled Lil' Buddies Pet Laser Toys (model 24496) because they contain button cell batteries that can be swallowed by young children, posing a serious injury or death risk. The toys—white with small blue paw prints—also have tentacle ends that can choke small children and violate safety standards for children's toys. No injuries have been reported yet.
SeriousCPSCApr 16, 2026
Stop using ATOYUS activity cube toyATOYUS wooden activity cubes sold on Amazon contain small parts that can detach, including xylophone screws, clock hands, and mallet ends. These parts pose a choking risk for young children. The toys were sold between January and February 2026.
SeriousCPSCApr 16, 2026
Remove batteries from Sanlebi Pet Vet Playset immediatelyThe Sanlebi Pet Vet Playset (model MX094) contains button cell batteries in the toy nail grinder and otoscope that children can easily access. Button cell batteries can cause serious injury or death if swallowed. About 4,650 playsets were sold on Amazon between June 2025 and January 2026.
SeriousCPSCApr 16, 2026
- Check Tornier HRS Max shoulder implant parts
Tornier, Inc. recalled three shoulder implant parts that were incorrectly labeled as compatible with the Tornier HRS Max system. These parts actually work only with the older Tornier HRS system and will not fit properly in HRS Max procedures. A total of 233 units with specific lot numbers were distributed nationwide.
ModerateFDAApr 15, 2026Tornier
Stop using Goregent infant walkers immediatelyGoregent-branded infant walkers sold on Amazon can fit through standard doorways and do not stop at the edge of stairs, creating a serious fall risk. About 90 walkers with model number 901 and a yellow production label dated November 2025 are affected. No injuries have been reported yet.
SeriousCPSCMar 19, 2026
- Valley Springs bottled water recalled for insanitary bottling conditions
Valley Springs/Artesian Gold recalled three 1-gallon water products sold as Valley Springs 100% Natural Bottled Water (including a fluoride-added version) and Valley Springs Steamed Distilled Water. The water was bottled under insanitary conditions. The products were distributed in Illinois and Wisconsin, and no injuries have been reported.
ModerateFDAMar 4, 2026Valley Springs Artesian Gold3 products
TheKiddoSpace 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 ToysThe 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.
CPSCFeb 26, 2026
Stop using TheKiddoSpace handwriting kitsTheKiddoSpace children's handwriting practice kits contain pens with lead levels that exceed federal safety limits. The pens come in both block and cursive alphabet versions sold online. Lead can be toxic if children ingest it.
SeriousCPSCFeb 26, 2026
- Check Medline surgical drapes for sterilization defects
Medline Industries recalled multiple surgical drape products due to calibration problems with sterilization equipment. While the drapes went through sterilization and packaging, equipment calibration issues may have compromised their sterility. No injuries have been reported.
ModerateFDAFeb 25, 202642 products
- Stop using affected Bard Broviac and Hickman catheters
Bard Peripheral Vascular is recalling multiple central venous catheter trays and kits because the outer packaging may be damaged, which could compromise the sterile barrier that protects the medical device. The recall affects several Broviac and Hickman catheter products with specific lot numbers manufactured between April 2028 and August 2030.
ModerateFDAFeb 25, 2026
Return Meijer children's sleepwear to storeMeijer is recalling about 211,520 units of Lullaby Lane and MCS branded one-piece footed sleepwear in sizes 12–24 months because they fail to meet mandatory flammability standards for children's sleepwear. The fabric can catch fire more easily than allowed, posing a burn risk to young children. No injuries have been reported yet.
SeriousCPSCFeb 19, 2026
- Fujirebio Lumipulse Alzheimer's blood tests recalled for false results
Fujirebio is recalling seven Lumipulse plasma test products used to measure amyloid and pTau217 for Alzheimer's disease. The tests can produce falsely elevated results, which may wrongly classify a patient as having Alzheimer's-related amyloid pathology or lead to unneeded additional testing. No injuries have been reported.
ModerateFDAFeb 11, 2026Fujirebio7 products
- Stop using Vortex Surgical laser probes
Vortex Surgical laser probes used in eye surgery may have small voids or gaps in their sterile packaging seals. If the seal is compromised, bacteria could contaminate the sterile device and cause infection during surgery. No injuries have been reported so far.
ModerateFDAFeb 11, 2026Vortex Surgical13 products
Stop using Hobby Lobby plush toys with clipsThe legs on these Hobby Lobby plush toys can detach from the body, releasing small beads inside. Young children could choke on these beads. One incident has been reported, but no injuries so far.
SeriousCPSCJan 29, 2026
- Check your GE Omni Legend PET scanner
Certain GE Healthcare Omni Legend PET scanners may occasionally produce streaking artifacts in scan images. This visual distortion appears as lines in the images displayed on the scanner console and could affect image quality used for clinical diagnosis.
ModerateFDAJan 28, 2026
- Copan DTT sputum transfer tubes recalled for reagent failure
Copan is recalling two versions of its 1 ml DTT liquid-phase transfer tubes used to liquefy respiratory specimens, covering 245,700 units in total. The company cannot guarantee the treatment reagent will work properly, so specimen liquefaction may not be reliable. The tubes were distributed to 14 states, and no injuries have been reported.
ModerateFDADec 24, 2025Copan2 products
- Pet Allergy Test
Distribution without premarket approval/clearance.
FDADec 10, 2025Get Tested92 products
- Brand Name: Vacuette Product Name: 8 ml CAT Serum Separator Clot Activator Model/Catalog Number: 455071P Product Description: Greiner VACUETTE Blood Collection Tube with Clot Activator and Gel Separator and Standard Stopper (16 x 100 mm, 8ml)
Some of the Vacuette¿ CAT Serum Separator Clot Activator tubes were manufactured without gel separator, which could yield erroneous assay results and require the patient to return to the lab for recollection or repeat testing. This may result in delayed diagnosis, cause a delay in clinical decision-making or treatment and in some rare cases, yield incorrect results from less stable parameters.
FDANov 26, 2025