immediate action Recalls

2,756 recalls tagged with “immediate action”.

Food & Beverages
HIGH
FDA FOOD

ONE FROZEN Recalls Good and Gather Southwest-Style Burrito Bowl Blend for Shrimp Allergen (2025)

ONE FROZEN recalled 57,240 bags of Good and Gather Southwest-Style Burrito Bowl Blend sold nationwide after discovering undeclared shrimp. The product may contain shellfish due to cross-contact risk in a facility that also handles shellfish and other allergens. Consumers should not eat the product and should contact ONE FROZEN for a refund or replacement.

ONE FROZEN
Product may
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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
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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
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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
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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
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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
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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
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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
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Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems Recalled 32,433 Orthopedic Surgical Kits Over Re-Gassing Risk (2025)

American Contract Systems recalled 32,433 medical convenience kits sold through multiple retailers nationwide in SD, IA, MN, WA and IL. The devices were re-gassed after a nonconformance in the Ethylene Oxide sterilization process. The sterilization cycles have not been validated, so quality, safety and effectiveness cannot be confirmed. Consumers and healthcare providers should stop using the kits

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

Lutronic XERF EFFECTOR 60 Electrosurgical Unit Recalled for Manufacturing Defects (2025-2026 Models)

Lutronic recalled 7,490 XERF EFFECTOR 60 electrosurgical units distributed worldwide, including several U.S. states, after manufacturing defects surfaced between April 1 and August 20, 2025. The defect can cause adverse events for patients. Healthcare providers and patients should stop using the device immediately and follow the manufacturer’s recall instructions.

Lutronic
Manufacturing defects
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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
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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
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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
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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
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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
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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
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Food & Beverages
HIGH
FDA FOOD

Organicare Nature's Science FemiClear Daily Bladder Strength Recall 15,075 Bottles in 2025 Over E. C

Organicare Nature's Science recalled 15,075 bottles of FemiClear Daily Bladder Strength, sold in retail stores across all 50 states and Puerto Rico and online. The recall cites microbial contamination with Escherichia coli O7:K1 and E. coli 1303. Consumers should stop using the product and contact Organicare Nature's Science for a refund or replacement.

Organicare Nature's Science
Microbial contamination
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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
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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
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Tag Statistics

Total Recalls
2,756

Related Tags

kitchenpoisoning riskstop use immediatelyreturn for refundreplacement availableholiday productfda regulatedelectrical hazardchemical hazardrepair availablefederal law violationcpsc regulated