chemical hazard Recalls

1,003 recalls tagged with “chemical hazard”.

Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems Recalls 32,433 Medical Convenience Kits Over Re-Gassing Risk (2025)

American Contract Systems recalled 32,433 medical convenience kits sold through multiple retailers nationwide. The devices were re-gassed after a nonconformance in the Ethylene Oxide gas injection process and have not been validated for exposure to multiple sterilization cycles. Healthcare providers and patients should stop using these products immediately and follow the manufacturer's recall.

American Contract Systems
Identified products
Read more
Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems Recalling 32,433 UDPG88W PICC G-TUBE Pack in 2025 Recall

American Contract Systems recalled 32,433 UDPG88W PICC G-TUBE PACK medical kits nationwide after a nonconformance in Ethylene Oxide sterilization led to re-gassing. The devices have not been validated for multiple sterilization cycles. Healthcare providers and patients should stop using the kit immediately and follow recall instructions.

American Contract Systems
Identified products
Read more
Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems Recalls 32,433 Medical Convenience Kits Over EO Re-Gassing Risk (2025)

American Contract Systems Inc. recalls 32,433 medical convenience kits distributed nationwide to healthcare facilities in SD, IA, MN, WA, and IL. Re-gassed after a nonconformance occurred during Ethylene Oxide gas injection. The kits have not been validated for multiple sterilization cycles. Healthcare providers should stop using the devices immediately and follow recall instructions.

American Contract Systems
Identified products
Read more
Food & Beverages
HIGH
FDA FOOD

Pacific Coast Producers Halved Pears in Pear Juice Recall 2025 — 102 Cases Lead Contamination

Pacific Coast Producers recalled 102 cases of Halved Pears in Pear Juice Concentrate sold nationwide through Wegmans distribution after detecting potential lead contamination. The product is packaged in 15-ounce cans with Lot 6PJ 09 C2295 and UPC 077890747490. Consumers should stop using the product and contact Pacific Coast Producers for refund or replacement.

Pacific Coast Producers
Potential contamination
Read more
Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems High-Rire Recall: 32,433 Medical Convenience Kits Recalled for Re-GassedEO

American Contract Systems recalled 32,433 medical convenience kits nationwide after finding re-gassed devices from EO sterilization. The recall affects five product lines with UDI-DI codes and Lot numbers. The re-gassing process has not been validated for multiple sterilization cycles, calling into question product safety and effectiveness. Health providers and patients should stop using these kit

American Contract Systems
Identified products
Read more
Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems Recalls 32,433 Angio Packs Over Re-Gassed EO Sterilization (2025)

American Contract Systems is recalling 32,433 medical Angio Packs distributed nationwide in the United States. The devices were re-gassed after a nonconformance in the Ethylene Oxide gas injection process. Healthcare facilities and patients should stop using the devices and follow the manufacturer’s recall instructions.

American Contract Systems
Identified products
Read more
Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems High-Index Medical Kits Recalled for Re-Gassing After EO Sterilization Non

American Contract Systems recalled 32,433 medical convenience kits nationwide in the United States after re-gassing sterilization cycles. The recall covers multiple packs including HEART PACK and PACEMAKER PACK with 2025 recall date. The safety issue centers on EO gasset validation failures after a nonconformance during initial gas injection. Stop using immediately and follow recall instructions.

American Contract Systems
Identified products
Read more
Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems Labor Delivery Packs Recalled for Re-Gassed Sterilization Flaw (2025)

American Contract Systems recalled 32,433 labor and delivery packs nationwide in the United States, including the states of South Dakota, Iowa, Minnesota, Washington and Illinois. Re-gassing occurred after a nonconformance in the Ethylene Oxide gas injection process. The affected packs have not been validated for exposure to multiple sterilization cycles. Hospitals and health systems should stop使用

American Contract Systems
Identified products
Read more
Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems IHDC30R D AND C PACK Medical Kits Recalled Over Re-Gassing (32,433 Units,

American Contract Systems recalled the IHDC30R D AND C PACK medical convenience kits distributed nationwide in the United States. The recall stems from a nonconformance during Ethylene Oxide gas injection that led to re-gassing. The products have not been validated for exposure to multiple sterilization cycles. Health safety cannot be confirmed for re-gassed units. Stop using them and await recall

American Contract Systems
Identified products
Read more
Food & Beverages
HIGH
FDA FOOD

Gospodarstwo Pasieczne Sadecki Bartnik Bee Pollen 200g Recall for Pyrrolizidine Alkaloids (2025)

Gospodarstwo Pasieczne Sadecki Bartnik recalled 336 jars of Bee Pollen sold in Illinois after tests detected pyrrolizidine alkaloids. The product contains detectable pyrrolizidine alkaloids. Consumers should not consume the product and should contact the producer by telephone for refund or replacement.

Gospodarstwo Pasieczne Sadecki Bartnik
detectable pyrrolizidine
Read more
Food & Beverages
HIGH
FDA FOOD

Pacific Coast Producers Pears Halves in Pear Juice Recall 2025 for Lead Contamination

Pacific Coast Producers recalled 1,836 cases of Pears Halves in Pear Juice from Concentrate distributed by Walmart. The product may be contaminated with lead, a heavy metal hazard. Consumers should not eat this product and should contact Pacific Coast Producers for a refund or replacement by telephone.

Pacific Coast Producers
Potential contamination
Read more
Food & Beverages
HIGH
FDA FOOD

Pacific Coast Producers Fruit Cocktail Recalled for Lead Contamination in 15 oz Cans (609 cases)

Pacific Coast Producers recalled 609 cases of Fruit Cocktail in 15 oz cans distributed by Wegmans Food Markets over lead contamination concerns. The recall cites potential contamination with lead. Consumers who purchased the product should not consume it and should contact Pacific Coast Producers for a refund or replacement.

Pacific Coast Producers
Potential contamination
Read more
Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems LKRA40G Radiology Pack Recalled Over Unvalidated Re-sterilization (HIGH)

American Contract Systems recalled 32,433 radiology packs after a nonconformance during EO gas injection. The items were re-gassed and not validated for multiple sterilization cycles. The recall is active as of 2025-10-22. US distribution included SD, IA, MN, WA, IL. Health risks prompt immediate removal from use.

American Contract Systems
Identified products
Read more
Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems Basic Biopsy Tray Recalled for Re-Gassing Hazard (32,433 Units) 2025Recall

American Contract Systems recalled 32,433 Basic Biopsy Trays nationwide after discovering re-gassing occurred following a nonconformance during Ethylene Oxide sterilization. The trays have not been validated for exposure to multiple sterilization cycles, so product quality and safety cannot be confirmed. Healthcare providers and patients should stop using the device immediately and follow theメーカー?

American Contract Systems
Identified products
Read more
Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems Recalls 32,433 Cardiac Cath Lab Kits Due to Re-Gassed Sterilization Risk (

American Contract Systems recalled 32,433 cardiac cath lab kits distributed nationwide to healthcare providers. The devices were re-gassed after a nonconformance in the Ethylene Oxide gas injection process. The kits have not been validated for exposure to multiple sterilization cycles and cannot be guaranteed safe.

American Contract Systems
Identified products
Read more
Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems Recalls 32,433 Basic Biopsy Trays Re-Gassed After EO Sterilization (2025)

American Contract Systems recalled 32,433 basic biopsy trays distributed nationwide in the United States. These trays were re-gassed after a nonconformance occurred during the initial Ethylene Oxide gas injection. The trays have not been validated for exposure to multiple sterilization cycles. Healthcare providers and patients should stop using affected trays and follow recall instructions.

American Contract Systems
Identified products
Read more
Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems Medical Convenience Kits Recalled for Re-Gassing Risk

American Contract Systems recalled 32,433 medical convenience kits after it was discovered they were re-gassed after sterilization failure. The sterilization process may compromise the product's quality, safety, and effectiveness. Healthcare providers must stop using these kits immediately and follow up with the manufacturer for instructions.

American Contract Systems
Identified products
Read more
Health & Personal Care
HIGH
FDA DRUG

Zydus Lifesciences Chlorpromazine Hydrochloride Tablets 50 mg 100-count Recall 2025

Zydus Lifesciences and Northstar Rx LLC recall Chlorpromazine Hydrochloride Tablets, 50 mg, 100-count bottles distributed nationwide in the United States. The recall cites CGMP deviations and the presence of N-Nitroso Desmethyl Chlorpromazine above the acceptable intake limit. Stop using the product immediately and contact your healthcare provider or Zydus Pharmaceuticals (USA) Inc for guidance.

Zydus Lifesciences
CGMP Deviations:
Read more
Health & Personal Care
HIGH
FDA DRUG

Zydus Chlorpromazine Hydrochloride 10 mg Tablets Recalled for Nitrosamine Impurity (2025)

Zydus Lifesciences and Zydus Pharmaceuticals US recall Chlorpromazine Hydrochloride Tablets, 10 mg, 100-count bottles sold nationwide in the United States after detecting an impurity above acceptable intake. The impurity is N-Nitroso Desmethyl Chlorpromazine. Consumers should stop using the product immediately and contact the manufacturer for guidance.

Chlorpromazine Hydrochloride
CGMP Deviations:
Read more
Previous
12345...51
Next

Tag Statistics

Total Recalls
1,003

Related Tags

electrical hazardsuffocation riskinfant productadult productmandatory standard violationfda regulatedcpsc regulatedimmediate actionstop use immediatelyreturn for refundrepair availablereplacement available