Pet food and pet product recalls
1082 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.
- 2020-09-23FDA-FoodPonder FoodsClass IIPretty Thai brand Sweet Chili Sauce Net Wt 11.2 oz (317g) UPC 860043001224 packaged in a clear PET plastic bottle with a white label.
Potential to contain undeclared peanuts
- 2020-09-16FDA-DeviceSICAT GMBH & CO. KGClass IISICAT IMPLANT V2.0
A dentist found implant positions are not correctly exported from the implant planning software SICAT IMPLANT V2.0 - for the specific export format CMG.DXD.
- 2020-09-09FDA-FoodSundial Herbal ProductsClass II"SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***TRUMPET LEAF***1 oz.***USES: DIABETES, ASTHMA, CONGESTION, SKIN BATH, ULCERS, SORES, PARKINSON'S DISEASE, KIDNEY***"; packaged in clear plastic zip-top bags
Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.
- 2020-09-09FDA-FoodSundial Herbal ProductsClass II"SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***DOG BLOOD***1 oz.***USES: FIBROIDS, CYST, CLEANS WOMB, WOMAN IMBALANCE, PREVENT MISCARRIAGE***"; packaged in clear plastic zip-top bag
Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.
- 2020-09-04USDAPublic Health AlertDo not eat imported duck blood curds
Unfit for Human Consumption
- 2020-07-23CPSCPolaris Industries Inc., of Medina, Minn.Polaris Recalls Ranger Off-Road Vehicles and PRO XD and Bobcat Utility Vehicles Due to Crash Hazard (Recall Alert)
An improperly manufactured clutch component can cause the engine braking feature to fail, resulting in unexpected vehicle motion, posing a crash hazard.
- 2020-07-15FDA-DeviceCooperSurgical, Inc.Class IICOOPERSURGICAL Os FinderTM Cervical Dilator, Taper: 2.0 mm to 4.0 mm OD Length: 21.5 cm Box of 50 Part Number: 1176
Mislabeled: Printing on the top web or Tyvek lid of the individual product blister tray indicating that it contains a Pipet Current or Part Number MX140 and the display box indicating the correct Os FinderTM Cervical Dilators, Part Number 1176. The product in the individual product package is the correct Os Finder Cervical Dilator
- 2020-07-08FDA-DeviceArrow International IncClass IArrow AutoCAT2 Intra-Aortic Balloon Pump AEROAUTOCAT 2 WAVE, Product Code IAP-0535
A potential issue with a component within the above-referenced IABPs may impact the ability of the devices to operate. A Component within the IABP is susceptible to vibration failure resulting in fretting, charring, and discoloration of motor connector wires, which may result in pump alarms for System Error 3 and High Baseline presented on the screen of the IABP, and potential abrupt cessation of function or inability to start the IABP.
- 2020-07-08FDA-DeviceArrow International IncClass IArrow AutoCAT2 Intra-Aortic Balloon Pump AUTOCAT2 WAVE SPANISH, Product Code IAP-0500E
A potential issue with a component within the above-referenced IABPs may impact the ability of the devices to operate. A Component within the IABP is susceptible to vibration failure resulting in fretting, charring, and discoloration of motor connector wires, which may result in pump alarms for System Error 3 and High Baseline presented on the screen of the IABP, and potential abrupt cessation of function or inability to start the IABP.
- 2020-07-08FDA-DeviceArrow International IncClass IArrow AutoCAT2 Intra-Aortic Balloon Pump AUTOCAT2 WAVE, Product Code IAP-0500
A potential issue with a component within the above-referenced IABPs may impact the ability of the devices to operate. A Component within the IABP is susceptible to vibration failure resulting in fretting, charring, and discoloration of motor connector wires, which may result in pump alarms for System Error 3 and High Baseline presented on the screen of the IABP, and potential abrupt cessation of function or inability to start the IABP.
- 2020-07-08FDA-DeviceArrow International IncClass IArrow AutoCAT2 Intra-Aortic Balloon Pump AUTOCAT 2, Product Code IAP-0400
A potential issue with a component within the above-referenced IABPs may impact the ability of the devices to operate. A Component within the IABP is susceptible to vibration failure resulting in fretting, charring, and discoloration of motor connector wires, which may result in pump alarms for System Error 3 and High Baseline presented on the screen of the IABP, and potential abrupt cessation of function or inability to start the IABP.
- 2020-07-01CPSCSymbol Arts LLC, of Ogden, UtahBoy Scouts of America Recalls Cub Scout Activity Pins Due to Violation of the Federal Lead Content Ban
The pin's face and shaft contain levels of lead that exceed the federal lead content ban. Lead is toxic if ingested by young children and can cause adverse health issues.
- 2020-06-24FDA-DeviceDefibtech, LLCClass IIDDU-2450 Lifeline ECG Model Numbers DDU-A2450EN DDU-E2450DE DDU-E2450EN DDU-E2450FR DDU-E2450TH Cat. No. DCF-A2460EN DCF-A2463EN DCF-E2460DE DCF-E2460EN DCF-E2460FR DCF-E2460TH UDI 00815098020287, 00815098020317 Automated External Defibrillators (AED) are indicated for use on victims of sudden cardiac arrest (SCA) who are: - unconscious and unresponsive, not breathing or not breathing normally.
A component issue may cause the AED to abort a shock delivery or reset unexpectedly, which may cause an affected device to fail to delivery shock, and/or to fail to deliver shock in range.
- 2020-06-24FDA-DeviceDefibtech, LLCClass IIDDU-2400EN Lifeline PRO, UDI 00815098020270 - Product Usage: Automated External Defibrillators (AED) are indicated for use on victims of sudden cardiac arrest (SCA) who are: - unconscious and unresponsive, not breathing or not breathing normally.
A component issue may cause the AED to abort a shock delivery or reset unexpectedly, which may cause an affected device to fail to delivery shock, and/or to fail to deliver shock in range.
- 2020-06-24FDA-DeviceDefibtech, LLCClass IIDDU-2300 Lifeline/ReviveR View, Model Numbers DDU-C2300EN, DDU-C2300CA, DDU-A2300EN, DDU-E2300EN Catalog Numbers CCD-A1006RX CCD-A1013EN CCD-A1015EN DCF-A2310EN DCF-A2310RX DCF-A2313EN DCF-C2310CA DCF-C2310EN DCF-E2310CA DCF-E2310EN UDI 00815098020201, 00815098020225, 00815098020232 Product Usage: Automated External Defibrillators (AED) are indicated for use on victims of sudden cardiac arrest (SCA) who are: - unconscious and unresponsive, not breathing or not breathing normally
A component issue may cause the AED to abort a shock delivery or reset unexpectedly, which may cause an affected device to fail to delivery shock, and/or to fail to deliver shock in range.
- 2020-05-27CPSCPrimark US Corp., of Boston, Mass.Primark Recalls Kitten Heel Court Shoes Due to High Levels of Chromium; Risk of Skin Irritation
The leather insock in the shoes has elevated levels of Chromium VI, posing a risk of skin irritation.
- 2020-05-13FDA-DeviceICU Medical, Inc.Class IIREF: AH7117 111" 10 Drop Admin Set w/2 Inj Sites, Rotating Luer, Sterile R, For Veterinary Use Only, (01) 1 0887709 051475
There is a potential that IV administration sets contain a 15 drops/mL drop cannula instead of a 10 drops/mL drop cannula within the drip chamber. An infusion set with an incorrect drop cannula could result in inaccurate delivery of the intended infusion volume (under-delivery). This could result in under-delivery of critical medication which may lead to serious adverse health consequences.
- 2020-04-22FDA-DeviceShanghai United Imaging Healthcare Co., Ltd.Class IIPositron Emission Tomograpy and Computed Tomography System, Model: uMI 550, with software version R001.3.0.0.750505, Rx Only, CE 0197, UDI: (01)06971576832026 - Product Usage: This system is intended to be operated by qualified healthcare professionals to assist in the detection, localization, diagnosis, staging, restaging, treatment planning and treatment response evaluation for diseases and disorders in, but not limit to, oncology, cardiology and neurology.
Potential sporadic software bugs in R001.3.0.0.750505 software version may cause an issue with the PET acquisition raw data causing reconstruction problems during PET/CT scanning and could possibly cause rescans of patients with additional dose.
- 2020-02-12FDA-DeviceB. Braun Medical, Inc.Class IISafeline Y-Type Blood Set, Catalog Number V2500
Potential for leakage at the joint between the blood filters and tubing
- 2020-02-12FDA-DeviceB. Braun Medical, Inc.Class IISafeline Y-Type Blood Set, Catalog Number NF5140
Potential for leakage at the joint between the blood filters and tubing
- 2020-01-30CPSCPolaris Industries Inc., of Medina, Minn.Bobcat Company Recalls Utility Vehicles (UTVs) Due to Collision and Crash Hazard (Recall Alert)
The rear brake line can become punctured causing the brakes to fail, posing a collision and crash hazard.
- 2019-12-25FDA-FoodHuy Fong Foods, IncClass IIISiracha HOT Chili Sauce Net Wt. 28 oz. (1 lb. 12 oz.) (793 g); Net Wt. 17 oz. (1 Lb. 1 oz.) in PET Plastic bottles UPC: 0 24463 06116 Huy Fong Foods, Inc. 4800 Azusa Rd. Irwindale, CA 91706
Firm received complaint of Siracha sauce bulging at top seal and exploding upon removing seal
- 2019-11-27FDA-DeviceNucryo Vascular Inc.Class IIThe PolarCath Balloon Catheter consists of a coaxial catheter shaft with two concentric, non-compliant balloon systems mounted at the distal tip (balloon within a balloon design). The catheter is available in various working lengths and appropriate balloon diameters and lengths. The balloon has radiopaque markings to assist in balloon placement and to visualize proper expansion of the inflated balloon. The catheter tip is tapered to facilitate entry into peripheral arteries and across lesions. T
Peripheral Dilation Catheters that were E-Beam Sterilized were inadvertently mislabeled with EO sterilized labels.
- 2019-11-04USDAClass IDo not eat Cay Thi Queentrees black chicken
Import Violation
- 2019-10-25USDAClass IIDo not eat Taylor's Sausage products
Mislabeling
- 2019-09-19CPSCStrom Packaging Co. LTD, of ChinaExploding Kittens Recalls Safety Goggles Sold with Extreme Edition Dodgeball Game Sets Due to Laceration Hazard; Sold Exclusively on Kickstarter (Recall Alert)
The goggles contain glass lenses, posing a laceration hazard if shattered.
- 2019-09-03CPSCThe Beaufort Bonnet Company, of Lexington, Ky.The Beaufort Bonnet Company Recalls Handmade Knit Dolls Due to Injury Hazard
A sewing needle was discovered in the stuffing of one of the handmade knit dolls, posing a puncture injury hazard.
- 2019-08-27CPSCAt Home Procurement, of Plano, TexasAt Home Recalls Shag Rugs Due to Violation of Federal Flammability Standard; Fire Hazard
The recalled large shag rugs fail to meet the federal flammability standard for carpets and rugs, posing a fire hazard. The small shag rugs fail to meet federal labeling requirements. Small rugs are not required to meet the federal flammability standard; however, they are required to be permanently labeled with the following statement: "FLAMMABLE (FAILS U.S. DEPARTMENT OF COMMERCE STANDARD FF 2-70): SHOULD NOT BE USED NEAR SOURCES OF IGNITION."
- 2019-08-14FDA-FoodMott's LLPClass IIIPenafiel Mineral Spring Water 600mL (20.3 FL OZ) and Penafiel Mineral Spring Water 1.5 L (50.7 FL OZ) packaged in clear PET bottles, 12 units per case UPC 078000200249 and 078000200294
Elevated levels of inorganic arsenic
- 2019-07-31FDA-FoodC & S Wholesale Grocers, Inc.Class IIFRESHPET SELECT GRAIN FREE SMALL - REFRIGERATED DOG FOOD - 1LB, UPC: 2797501204
Products were not held at an appropriate temperature due to a mechanical malfunction during transportation.
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