immediate action Recalls

2,756 recalls tagged with “immediate action”.

Food & Beverages
HIGH
FDA FOOD

Great Lakes Cheese Co Recalls 4,298 Cases of Pizza-Style Shredded Cheese Blends for Metal Fragments

Great Lakes Cheese Co Inc recalls 4,298 cases of pizza-style shredded cheese blends sold through retailers nationwide after metal fragments were found in supplier raw material. The defect involves potential metal fragments that could contaminate the cheese. Consumers who may own any of the affected products should not consume them and should contact Great Lakes Cheese Co for refund or replacement.

Great Lakes Cheese Co
Potential metal
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Food & Beverages
HIGH
FDA FOOD

Good & Gather Mozzarella & Parmesan Shredded Cheese Blend Recalled in 1,850 Cases (2026)

Target recalls 1,850 cases of Good & Gather Mozzarella & Parmesan shredded cheese blend sold at Target stores after metal fragments were found in a supplier ingredient. The issue involves potential metal fragments from a supplier raw material. Consumers should not consume this product and should contact Great Lakes Cheese Co for refund or replacement information.

Good & Gather
Potential metal
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Food & Beverages
HIGH
FDA FOOD

Food Club Finely Shredded Pizza Style Four Cheese Blend Recalled for Metal Fragments in 117 Cases (-

Food Club recalled 117 cases of Finely Shredded Pizza Style Four Cheese Blend, sold at multiple retailers nationwide, after potential metal fragments were found in a supplier raw material. The 8-ounce packages contain mozzarella, provolone, parmesan and romano cheeses and carry UPC 3680017231. Consumers should not eat this product and should contact Great Lakes Cheese Co for refund or replacement.

Food Club
Potential metal
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Health & Personal Care
HIGH
FDA DRUG

Advanced Pharmaceutical Technology Recalls Testosterone Pellets Due to Contamination Risk

Advanced Pharmaceutical Technology recalled 22,843 cartons of TESTO-100 CIII testosterone pellets on October 3, 2025. The recall follows a risk of microbial contamination that could compromise product sterility. Consumers and healthcare providers should stop using the product immediately and seek guidance.

Advanced Pharmaceutical Technology
Lack of
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Recalled Evermore Surprise Egg – Yellow Wrap
HIGH
CPSC

In Motion Design Recalls Evermore Surprise Eggs for Lead Hazard

In Motion Design recalled Evermore Surprise Eggs due to lead content above federal limits. The recalled eggs were sold with yellow, pink or green wrap and include a gold egg containing seven toys, including a toy airplane. Consumers should stop using the product and return it for a full refund.

In Motion Design
The toy
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Food & Beverages
HIGH
FDA FOOD

Leprino Foods Recalls 5,453,442 Lb Bulk Mozzarella Over Stainless Steel Pieces (2025)

Leprino Foods recalled 5,453,442 pounds of LMPS bulk mozzarella distributed to Ohio, Tennessee, Texas, Utah and Wisconsin after the FDA enforcement notice. The recall cites the possible presence of stainless steel pieces in the product. Consumers should not consume the mozzarella and should contact Leprino Foods for refund or replacement information.

Leprino Foods
Possible stainless
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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

DEMERS FOOD GROUP Recalls Scott & Jon's Shrimp Scampi with Linguine 9.6 oz for Listeria (2025)

DEMERS FOOD GROUP LLC is recalling Scott & Jon's Shrimp Scampi with Linguine, 9.6 oz, sold nationwide. The linguine component, manufactured by Nate's Fine Foods LLC, was recalled for Listeria monocytogenes and linked to an ongoing outbreak. Consumers should not consume the product and should contact DEMERS FOOD GROUP LLC for refund or replacement using email, fax, letter, press release, telephone,

Demers Food Group
Contains Linguine
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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 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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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

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

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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Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Nederland 718096 Zenition 50 Interventional X-Ray System Recalled in 2025

Philips Medical Systems Nederland B.V. recalled 29 Zenition 50 interventional fluoroscopic x-ray systems distributed in 14 countries. The defect is corrosion of the IITV control board that may cause loss of imaging functionality or poor image quality. Healthcare providers and patients should stop using the device and follow manufacturer instructions for recall remediation.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Over time
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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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Tag Statistics

Total Recalls
2,756

Related Tags

metalkitchenchemical hazardstop use immediatelyreturn for refundreplacement availablefda regulatedcpsc regulatedinfant producttoddler productadult productpet related