cpsc regulated Recalls

2,056 recalls tagged with “cpsc regulated”.

Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical Recalls 18,984 IV Administration Sets Over Backflow Hazard

B Braun Medical recalled 18,984 IV administration sets after discovering a potential for backflow of medication from secondary IV containers into primary containers. This defect creates a high risk of medication errors and occlusion. Patients and healthcare providers should stop using these sets immediately and contact B Braun Medical for further instructions.

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

B. Braun Medical Recalls 12,320 IV Burette Sets Over Backflow Risk (2025)

B. Braun Medical Inc. is recalling 12,320 burette sets worldwide used with Infusomat Space, Outlook Pump, and Vista Basic Pump. The device can allow backflow from secondary IV containers into primary containers and may fail to prime. Hospitals and clinics should stop using the device immediately and follow the recall instructions.

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

B Braun Medical ADDitIV Sets Recalled for High Backflow and Occlusion Risk, 43,900 Units Worldwide

B Braun Medical Inc. recalls 43,900 ADDitIV gravity and pump administration sets. The recall covers catalog numbers V1443, V1447, V1448, and V1484. The issue is backflow of medication from secondary IV containers into primary containers and inability to prime the line. Patients and healthcare providers should stop using these devices immediately and follow recall instructions.

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

B Braun Medical IV Administration Set Recall Affects 2,544 Units Worldwide

B Braun Medical Inc recalled 2,544 IV administration sets due to risk of backflow from secondary piggyback containers into primary IV lines and inability to prime. The recall covers products used with BBMI Infusomat Space, Outlook, and Vista Basic pumps and distributed worldwide including the US, Canada, Germany, Guatemala and Singapore. Patients should stop using the device immediately and follow

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

BBraun Medical IV Administration Set Recalled for Backflow and Occlusion Risk (490491, 2025)

BBraun Medical Inc recalls 960 IV administration sets distributed worldwide due to backflow risk and inability to prime. The recall affects the IV administration set catalog number 490491 with UDI-DI 04046955086931. The device can allow medication to flow from secondary piggyback containers into primary IV containers and may not prime properly. Stop using immediately and follow recall instructions

BBraun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical IV Administration Set Recall for 4,488 Units in 2025

B Braun Medical recalled 4,488 IV administration sets distributed worldwide, including the United States, Canada, Germany, Guatemala and Singapore. The devices risk backflow from secondary (piggyback) IV containers into primary containers and may be unable to prime due to occlusion. Healthcare facilities and patients should stop using immediately and follow recall instructions from the maker.

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

B. Braun Medical Inc. IV Administration Set Recall for 1,080 Units in 2025 recall

B. Braun Medical Inc. recalls 1,080 IV Administration Sets used with Infusomat Space, Outlook, and Vista Basic pumps. The recall addresses backflow from secondary piggyback containers into primary IV containers and an inability to prime (occlusion). Health care providers and patients should stop using the devices immediately and follow the manufacturer’s recall instructions.

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

B. Braun Medical Recalls 31,392 IV Administration Sets for Backflow Risk (2025)

B. Braun Medical Inc. recalls 31,392 IV administration sets used with Infusomat Space and other pumps worldwide. The device may allow backflow from piggyback containers into primary IV lines and cannot be primed. Hospitals and healthcare providers should stop using the device immediately and follow recall instructions.

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

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

B Braun Medical recalled 135,000 IV administration sets used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump, sold worldwide to hospitals and other healthcare providers. The devices pose a backflow risk from secondary to primary IV containers and can fail to prime. Health care facilities should stop using the affected sets and follow the manufacturer’s recall guidance.

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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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Anesthesia IV Set Recalled for Backflow Risk — 19,392 Units, 2025 Recall

B. Braun Medical recalled 19,392 Anesthesia IV Sets used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. The devices present a risk of backflow of medication from secondary piggyback IV containers into the primary IV line and an inability to prime. Hospitals and providers 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

Moonlight Packing Recalls Peaches Over Listeria Contamination

Moonlight Packing Corp. recalled 46,048 cases of peaches on October 28, 2025. The recall stems from potential contamination with Listeria monocytogenes. Consumers should not eat the affected product and should seek a refund.

Moonlight Packing
Potential contamination
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Food & Beverages
HIGH
FDA FOOD

India's Fine Foods Recalls Cookware Over Lead Contamination Risk

India's Fine Foods recalled 8 pieces of cookware on October 28, 2025, due to potential lead contamination. The affected products could pose a serious health risk to consumers. The recall affects products distributed in California and Washington.

India's Fine Foods
Potential contamination
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Food & Beverages
HIGH
FDA FOOD

Moonlight Packing Recalls Peaches Over Listeria Contamination Risk

Moonlight Packing Corp. recalled 483,973 cases of yellow peaches on October 28, 2025, due to potential Listeria contamination. Consumers should not consume the product and are advised to seek refunds. The peaches were distributed across multiple states and in Canada and Mexico.

Moonlight Packing
Potential contamination
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Food & Beverages
HIGH
FDA FOOD

Moonlight Packing Recalls Peppermint Peach Over Listeria Risk

Moonlight Packing Corporation recalled 439 bags of Peppermint Peach on October 28, 2025, due to potential Listeria monocytogenes contamination. The affected product weighs 2.25 lbs and may pose a serious health risk to consumers. The recall includes products distributed across multiple states and internationally.

Moonlight Packing
Potential contamination
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Health & Personal Care
HIGH
FDA DEVICE

Illumina NextSeq 550Dx Reagent Kits Recalled for Leaky Flow Cells Affecting 11,916 Units Worldwide

Illumina recalled 11,916 NextSeq 550Dx reagent kits and flow cells worldwide after identifying a gasket defect that can leak during sequencing. The issue may cause run failures, no or insufficient data output, instrument fluidics clogs and potential exposure to toxic substances. Healthcare providers and users should stop using the affected kits and await recall instructions from Illumina.

Illumina
An instrument
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Food & Beverages
HIGH
FDA FOOD

Moonlight Packing Issues Recall for Peppermint Peaches Due to Listeria

Moonlight Packing Corporation recalled 2,622 cases of sticker labels for loose bulk peppermint peaches on October 28, 2025. The recall stems from potential contamination with Listeria monocytogenes. Consumers should not consume this product and should contact the company for a refund or replacement.

Moonlight Packing
Potential contamination
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Health & Personal Care
HIGH
FDA DRUG

Agebox iKids-Growth Capsules Recalled Over Undeclared Ingredient

AGEBOX Inc. recalled 665 bottles of iKids-Growth capsules on October 28, 2025, due to undeclared ibutamoren. The product was marketed without an approved NDA/ANDA. Consumers should stop using the product immediately and contact Agebox for guidance.

Agebox
Marketed Without
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Tag Statistics

Total Recalls
2,056

Related Tags

burn riskelectrical hazardimmediate actionreturn for refundstop use immediatelyreplacement availablefda regulatedchemical hazardsuffocation riskinfant producttoddler productadult product