chemical hazard Recalls

1,003 recalls tagged with “chemical hazard”.

Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical Inc. Recalls 28,344 IV Administration Sets Linked to Backflow and Occlusion Risks (Z

B Braun Medical Inc. recalls 28,344 IV administration sets used with several BBMI infusion pumps after reports of backflow and occlusion risks. The recall covers a catalog number 470179 device distributed worldwide including the U.S., Canada, Germany, Guatemala and Singapore. The issue involves potential backflow from secondary IV containers into primary containers and the inability to prime the管.

BBraun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical IV Set Recall Affects 32,436 Units Over Backflow and Occlusion Risks (2025)

B Braun Medical Inc. recalled 32,436 Anesthesia IV Sets used with Infusomat Space, Outlook Pump, and Vista Basic Pump after reports of backflow risk and occlusion. The recall covers catalog numbers 490189 and 490226 distributed worldwide, including the US, Canada, Germany, Guatemala and Singapore. Consumers should stop using the device immediately and follow manufacturer instructions for recall. A

BBraun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

BBraun Medical Inc. Recalled 104,784 Anesthesia IV Sets Over Backflow, Occlusion Risk

BBraun Medical Inc. recalled 104,784 Anesthesia IV Sets used with Infusomat Space, Outlook, and Vista Basic pumps. The recall cites backflow of medication from secondary to primary IV containers and a potential inability to prime. Health care providers should stop using the devices immediately and follow the manufacturer’s recall instructions for refund or replacement.

BBraun 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 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 Sets Recalled for Backflow Risk and Occlusion (2025)

B Braun Medical Inc. recalls 111,312 IV Administration Sets worldwide, including US and international markets, due to backflow risk and occlusion. The recall affects catalog numbers 490193 and 490326, used with Infusomat Space, Outlook, and Vista Basic pumps. Stop using immediately and follow recall instructions for refunds or replacements.

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

BBMIs Infusomat IV Administration Set Recall, 63,192 Units Worldwide for Backflow and Occlusion Risk

BBMI recalled 63,192 IV administration sets worldwide on Oct 29, 2025. The recall affects the IV administration set labeled as 490426 with UDIs listed. The defect is potential backflow from secondary to primary IV containers and an inability to prime. Patients and healthcare providers should stop using these devices immediately and follow the manufacturer’s recall instructions.

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

B. Braun Medical Recalls 32,500 Caresite Extension Sets for IV Pumps (2025)

B. Braun Medical recalled 32,500 Caresite Extension Sets used with Infusomat Space, Outlook, and Vista Basic IV pumps worldwide. The devices pose a backflow and occlusion risk in the primary IV line. Hospitals and healthcare providers 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 Vista IV Set Recall for 74,652 Units Over Backflow and Occlusion Risk

B Braun Medical Inc recalls 74,652 Vista IV sets used with Infusomat Space and Vista Basic Pumps due to backflow and occlusion risks. The recall affects devices distributed worldwide, including the US, Canada, Germany, Guatemala, and Singapore. Stop using the device immediately and follow manufacturer instructions.

BBraun Medical
Potential for
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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 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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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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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

India's Fine Foods Recalls Cookware Over Lead Contamination Risk

India's Fine Foods recalled 10 pieces of cookware on October 28, 2025, due to potential lead contamination. Consumers should not use the product and seek refunds or replacements. The recall affects cookware distributed in California and Washington.

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

Moonlight Packing Recalls White Peaches Over Listeria Risk

Moonlight Packing Corporation recalled 104 cases of white peaches on October 28, 2025, due to potential contamination with Listeria monocytogenes. The recall affects 12-2 lb. bags per case distributed across multiple states and in Canada and Mexico. Consumers should not consume the product and are urged to seek refunds or replacements.

Moonlight Packing
Potential contamination
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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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Tag Statistics

Total Recalls
1,003

Related Tags

fire hazardback to schoolelectrical hazardinfant producttoddler productadult productelderly productholiday productcpsc regulatedfda regulatednhtsa regulatedimmediate action