pet related Recalls

224 recalls tagged with “pet related”.

Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical Extension Set Recalled for 1,200 Units Over Backflow and Occlusion Risk (2025 Recall

B Braun Medical recalled 1,200 extension sets used with Infusomat Space large-volume pumps distributed worldwide to hospitals and clinics. The recall cites potential backflow from secondary IV containers into primary containers and an inability to prime (occlusion). Healthcare facilities should stop using the devices immediately and follow the recall instructions issued by the manufacturer.

B Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Rate Flow IV Set Recalled for 150,664 Units in 2025

B. Braun Medical recalled 150,664 Rate Flow IV Sets used with Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump. The devices are cataloged as 375258. The recall addresses a potential backflow from piggyback IV containers into primary containers and an inability to prime. Hospitals and healthcare providers should stop using the device immediately and follow the manufacturer’s rec

B. Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical IV Administration Set Recall: 5,100 Units Distributed Worldwide Over Backflow and Oc

B Braun Medical Inc. recalls 5,100 IV administration sets distributed worldwide, including the US, Canada, Germany, Guatemala and Singapore. The recall cites backflow of medication from piggyback containers into primary IV containers and an occlusion that prevents priming. Patients should stop use immediately and follow recall instructions.

BB Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical IV Administration Set Recall for Backflow Risk (490566) 2025

B Braun Medical recalled its IV Administration Set used with Infusomat Space Large Volume Pumps and related models. The recall cites backflow of medication from secondary to primary IV containers and an occlusion that prevents priming. Hospitals and clinicians should stop using the device immediately and follow manufacturer recall instructions.

B Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical IV Administration Set Recalled for Backflow Risk in 65,904 Units (2025)

B. Braun Medical recalled 65,904 IV Administration Sets used with Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump. The recall cites backflow of medication from secondary (piggyback) IV containers into primary containers and an inability to prime. Hospitals should stop using the devices immediately and follow the manufacturer's recall instructions.

B. Braun Medical
Potential for
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Food & Beverages
HIGH
FDA FOOD

Twin Sisters Creamery Whatcom Farmhouse Cheese Recalled for Potential Contamination (411 lbs, 2025)

Twin Sisters Creamery recalled 411 pounds of Whatcom Farmhouse cheese sold through Whole Foods Market after testing flagged potential STEC and E. coli O103 contamination. The recall is Class I. Consumers who bought this product should not eat it and should contact WFM Purchasing, LP for refund or replacement information.

Twin Sisters Creamery
Twin Sisters
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Health & Personal Care
HIGH
FDA DEVICE

Siemens Medical Solutions USA Recalls MAMMOMAT Inspiration Operator Table for Bus-Installation Risk

Siemens Medical Solutions USA recalls the MAMMOMAT Inspiration operator table. The recall covers six units worldwide, including three in the United States. The operator table was sold with a bus-installation kit and is not designed or released for bus installations. Stop using the device immediately and contact Siemens for instructions.

Siemens Medical Solutions USA
There were
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Health & Personal Care
HIGH
FDA DRUG

Bristol-Myers Squibb Opdualag Vial Recall for Sterility Risk: 12,778 Units (2025)

Bristol-Myers Squibb recalled 12,778 Opdualag single-dose vials nationwide after a lack of assurance of sterility was identified. The product is nivolumab and relatlimab-rmbw injection. The recall date is 2025-10-21. Healthcare providers should stop using affected lots and follow the recall letter guidance.

Opdualag
Lack of
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Recalled DR2A and DR2E Golf Cars
HIGH
CPSC

Yamaha Recalls 2017-2024 Golf Cars Over Brake Failure Crash Hazard (2025)

Yamaha recalled model year 2017-2024 DR2A and DR2E Personal Transportation Vehicles sold through Yamaha dealers nationwide from June 2018 through July 2025. The brake system may fail to engage, creating a crash hazard with potential for serious injury or death. Owners should stop using the recalled golf cars and contact an authorized Yamaha Golf Car dealer to arrange a free brake repair. Yamaha or

Yamaha
The recalled
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Recalled E-Z-GO Valor PTV
HIGH
CPSC

Textron E-Z-GO Recalls Personal Transportation Vehicles Over Fuel Leak Fire Hazard (2025)

Textron E-Z-GO recalled certain personal transportation vehicles due to a fuel-line leak that can spark a fire. The recall covers RXV Freedom and Valor PTVs from model years 2020-2025 and TXT Freedom and Valor PTVs from model years 2020-2022. Dealers will inspect and replace the fuel line at no cost, and owners should stop using the vehicles until inspected.

Textron E-Z-GO
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

DERMASENSOR DermaSensor 10101 Diagnostic Device Recalled for 9 of 343 Units (2025)

DermaSensor recalled 343 units of its DermaSensor 10101 diagnostic device distributed to medical practices across several states. The device may not meet specifications, producing incorrect results or delaying referrals for patients with suspicious skin lesions. Health care providers should stop using the device immediately and contact Dermasensor Inc for instructions.

DERMASENSOR
Potential for
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Health & Personal Care
HIGH
FDA DRUG

USV Private Olopatadine Eye Drops 0.1% Recalled in 8,952 Bottles (2025)

USV Private recalled 8,952 bottles of Olopatadine Hydrochloride Ophthalmic Solution USP 0.1%. The product was distributed nationwide in the United States. The defect is failure of impurities/degradation specifications due to an unspecified impurity exceeding the limit. Stop using immediately and contact USV Private Limited or a healthcare provider for guidance.

USV Private
Failed Impurities/Degradation
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Food & Beverages
HIGH
FDA FOOD

Sno Pac Foods Frozen Organic Spinach Recall Affects 4,006 Cases (2025)

Sno Pac Foods recalled 4,006 cases of Frozen Organic Spinach sold under Sno Pac Frozen Vegetables and Maika'i Keep Frozen. The spinach may be contaminated with Listeria monocytogenes. Consumers should not eat the product and should contact Sno Pac Foods for refund or replacement.

Sno Pac Foods
Organic Spinach
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Food & Beverages
HIGH
FDA FOOD

Great Lakes Cheese Co Recalls 4,298 Cases of Pizza-Style Shredded Cheese Blends for Metal Fragments

Great Lakes Cheese Co Inc recalls 4,298 cases of pizza-style shredded cheese blends sold through retailers nationwide after metal fragments were found in supplier raw material. The defect involves potential metal fragments that could contaminate the cheese. Consumers who may own any of the affected products should not consume them and should contact Great Lakes Cheese Co for refund or replacement.

Great Lakes Cheese Co
Potential metal
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Tag Statistics

Total Recalls
224

Related Tags

immediate actionstop use immediatelyreplacement availableexplosion riskback to schoolinfant productadult productteen productelderly productchemical hazardsuffocation riskelectrical hazard