stop use immediately Recalls

2,153 recalls tagged with “stop use immediately”.

Health & Personal Care
HIGH
FDA DEVICE

Abiomed Impella Controller Recall Aims to Address Cybersecurity Vulnerabilities Across 32 Product SK

Abiomed recalled 10,153 Automated Impella Controllers and related components due to potential cybersecurity vulnerabilities in the operating system. The recall spans multiple international product codes and was first issued for devices distributed nationwide and internationally. Providers should stop using the affected controllers and follow manufacturer instructions immediately.

Abiomed
Potential cybersecurity
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Health & Personal Care
HIGH
FDA DRUG

Camber Ketorolac Tromethamine Injection Recall 2025 for Glass Particulates

Camber Pharmaceuticals recalled Ketorolac Tromethamine Injection, USP, 60 mg/2 mL, 2 mL single-dose vials distributed nationwide in the United States. The recall is due to the presence of glass particulates. Healthcare providers and patients should stop using the product immediately and contact Aspiro Pharma Limited at 1-866-495-1995 for guidance.

Ketorolac Tromethamine
Presence of
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Food & Beverages
HIGH
FDA FOOD

Ocean's Kitchen Imitation Crab Meat Recall 2025 Over Botulism Risk — 496 Cases in WA

Ocean's Kitchen recalled 496 cases of imitation crab meat shredded, distributed in Washington state. The product is refrigerated and vacuum-packaged. The recall cites potential contamination with Clostridium botulinum due to temperature abuse during chilled storage. Consumers should not consume the product and should contact Oceans Kitchen for refunds or replacements.

Oceans Kitchen
The potential
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Health & Personal Care
HIGH
FDA DEVICE

B BRAUN MEDICAL STREAMLINE BLOODLINE SET FOR DIALOG Recalled 1,298,454 Units (2025)

B BRAUN MEDICAL recalled 1,298,454 STREAMLINE BLOODLINE SET FOR DIALOG devices nationwide in the United States after observations of micro-air bubbles and air-in-line alarms linked to damaged arterial and venous connectors. The defect increases the risk of air entering the bloodstream during dialysis. Patients and healthcare providers should stop using this device immediately and follow the recall

B BRAUN MEDICAL
The potential
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Health & Personal Care
HIGH
FDA DEVICE

SHENZHEN ATOMSTACK TECHNOLOGIES Recalls Laser Products Over Safety Hazard

SHENZHEN ATOMSTACK TECHNOLOGIES recalled material processing laser products on September 30, 2025, due to a missing remote interlock connector. This defect poses a high risk according to federal regulations. Consumers should stop using these devices immediately and follow manufacturer instructions for remedy.

SHENZHEN ATOMSTACK TECHNOLOGIES
Lack of
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Health & Personal Care
HIGH
FDA DRUG

AFCO Hand Sanitizer 5515 Recalled for Methanol Risk Nationwide (2025)

AFCO's hand sanitizer 5515 is being recalled nationwide through distributors and retailers. The recall cites cGMP deviations that left methanol risk unexcluded. Consumers and healthcare providers should stop using this product immediately and contact Acuity Specialty Products for guidance.

AFCO
cGMP deviations:
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Food & Beverages
HIGH
FDA FOOD

New Age International Signature Enoki Mushroom Recall 175 Boxes in NY Over Listeria (2025)

New Age International recalled 175 boxes of Signature brand Enoki Mushroom sold in New York after testing revealed possible Listeria monocytogenes contamination. The product may be contaminated with Listeria monocytogenes. Consumers who bought it should not eat it and should contact New Age International for refund or replacement information.

New Age International
Product may
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Health & Personal Care
HIGH
FDA DRUG

Medline 222,800 Alcohol Prep Pads Recalled for Subpotent Drug (2025)

Medline Industries recalled 222,800 alcohol prep pads nationwide on Sept. 29, 2025 due to subpotent potency. The pads are 2-ply, 70% isopropyl alcohol. Stop using immediately and contact Medline or your healthcare provider for guidance.

Medline Industries
Subpotent Drug
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Health & Personal Care
HIGH
FDA DRUG

Acuity Specialty Products Hand Sanitizer Recalled for Methanol Risk Due to Unperformed Component-LOT

Acuity Specialty Products recalled hand sanitizer products sold nationwide due to potential methanol presence. The recall covers Wyandotte, Sanifect E3 ethanol-based sanitizer products manufactured by AFCO. The issue stems from unperformed receipt testing on incoming alcohol components. Consumers and healthcare providers should stop use immediately.

Acuity Specialty Products
cGMP deviations:
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Food & Beverages
HIGH
FDA FOOD

Vicky IT Bona Fish Recall: 10 Lbs in NY Over Contamination Risks (2025)

Vicky IT recalled 10 pounds of Bona Fish distributed in New York after FDA enforcement flagged the product for serious safety hazards. The recall cites un-eviscerated fish that may be contaminated with Clostridia botulinum, along with mold and insect larvae. Consumers who bought Bona Fish should not consume it and should contact Vicky IT for a refund or replacement.

Vicky IT
Fish is
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Food & Beverages
HIGH
FDA FOOD

Reser’s Fine Foods Salad Kit Recalled for Listeria Contamination (2025)

Reser’s Fine Foods recalled 3,252 cases of Basil Pesto Bowtie Pasta Kit Item V, UPC 13454 38053, distributed in AZ, CA, CO and TX. The recall concerns potential contamination with Listeria monocytogenes. Consumers should not eat the product and should seek refund or replacement.

Reser’s Fine Foods
Salad Kits
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Food & Beverages
HIGH
FDA FOOD

Wholesale Produce Recall: Cut Fresh Melon Mix Recalled Over Listeria Contamination Risk (2025)

Wholesale Produce Supply LLC DBA recalled 307 cases of Cut Fresh Melon Mix due to potential Listeria monocytogenes contamination. The recall covers multiple Melon Mix products packed by WPS in Minneapolis and distributed to IA, IL, ND, NE, and WI. Consumers should not eat the product and should seek refunds or replacements.

WHOLESALE PRODUCE SUPPLY LLC
Potential Listeria
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Food & Beverages
HIGH
FDA FOOD

Reser’s Fine Foods Salad Kits Recalled Over Listeria Risk in 795 Cases Distributed Across 9 States

A high-risk recall affects 795 cases of Reser’s Fine Foods Basil Pesto Bowtie Pasta Kit distributed in Arizona, California, Colorado, Utah and Washington. The recall covers item #404736 with use-by dates in October 2025. Consumers should not consume these salad kits and should contact Reser’s for refunds or replacements.

Reser's Fine Foods
Salad Kits
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Health & Personal Care
HIGH
FDA DRUG

Dr. Reddy's Succinylcholine Chloride Injection Recall 2025 — 571 Vials Over OOS Preservative Drop

Dr. Reddy's Laboratories Inc. recalled 571 vials of Succinylcholine Chloride Injection, USP nationwide in the United States. The recall cites an out-of-specification result during six-month stability testing due to decreased preservative concentration. Healthcare providers and patients should stop using the product immediately and await guidance from the recall letter.

Succinylcholine
Out-of-Specification (OOS)
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Food & Beverages
HIGH
FDA FOOD

Albertsons Store-Made Ready Meals Smoked Mozzarella Penne Pasta Salad Recalled for Listeria monocyt—

Albertsons Companies is recalling Ready Meals Smoked Mozzarella Penne Pasta Salad sold under Carrs-Safeway, Eagle and Safeway banners in Alaska and 14 other states after the FDA linked the product to Listeria monocytogenes. The in-store Penne pasta ingredient recall prompted the action. Consumers should not eat the product and should contact Albertsons Companies LLC for refund or replacement.

Albertsons Companies
Listeria monocytogenes.
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Food & Beverages
HIGH
FDA FOOD

Albertsons Recalls Store-Made Basil Pesto Bow Tie Pasta Salad Over Listeria Risk (2025)

Albertsons Companies recalled store-made Basil Pesto Bowtie Pasta Salad sold under Carrs-Safeway, Eagle, and Safeway banners. A Listeria monocytogenes contamination was linked to a bowtie pasta ingredient. Consumers who bought the product in 15 states should not eat it and should contact Albertsons for refund or replacement.

Albertsons Companies
Listeria monocytogenes.
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Food & Beverages
HIGH
FDA FOOD

Albertsons Basil Pesto Bowtie Pasta Salad Recalled for Listeria in 2025

Albertsons Companies recalled Basil Pesto Bowtie Pasta Salad sold at banners including Andronico's Community, Markets, Pak'N Save, Safeway and Vons due to Listeria monocytogenes contamination. The recall involves a store-made deli item with a bowtie pasta ingredient. Consumers should not consume the product and should contact Albertsons Companies LLC for refunds or replacements.

Albertsons
Listeria monocytogenes.
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Food & Beverages
HIGH
FDA FOOD

Albertsons Basil Bowtie Pasta Salad Recalled for Listeria Risk (2025)

Albertsons Companies LLC recalls Ready Meals Basil Bowtie Pasta Salad sold under banners including Albertsons, Market, Amigos, Market Street and United in NM and TX. The recall is tied to Listeria monocytogenes contamination. Consumers should not eat this product and should contact Albertsons for refund or replacement.

Albertsons Companies
Listeria monocytogenes.
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Tag Statistics

Total Recalls
2,153

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