stop use immediately Recalls

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

Food & Beverages
HIGH
FDA FOOD

Albertsons Recalls Store-Made Spinach Bowtie Pasta Salad Over Listeria (2025)

Albertsons recalled store-made Spinach Bowtie Pasta Salad due to Listeria monocytogenes. The recall covers deli items made in-store with scale-labels across banners including Albertsons, Amigos, Market Street, United in NY and TX. Consumers should not eat the product and should contact Albertsons for refund or replacement.

Albertsons
Listeria monocytogenes.
Read more
Food & Beverages
HIGH
FDA FOOD

Wholesale Produce Supply LLC Recalls 307 Cases of Cut Fresh Fruit Mix for Listeria Risk (2025)

Wholesale Produce Supply LLC recalls 307 cases of Cut Fresh Fruit Mix sold through multiple retailers in Iowa, Illinois, North Dakota, Nebraska and Wisconsin. The recall covers two brand variations and multiple lot numbers with October 2025 expirations. Consumers should not consume the product and should contact Wholesale Produce Supply LLC DBA for refund or replacement information.

Wholesale Produce Supply LLC
Potential Listeria
Read more
Recalled RELIEVE Numbing Cream – Outer Packaging
HIGH
CPSC

Mad Rabbit RELIEVE Lidocaine Numbing Cream Recalled for Non‑Child-Resistant Packaging

Mad Rabbit recalls RELIEVE lidocaine numbing cream due to non‑compliant packaging that could allow poisoning of young children. The recall covers a product sold under the Mad Rabbit brand and issued on 2025-09-25. The packaging does not meet the Poison Prevention Packaging Act requirement for child resistance. Consumers should stop using the product immediately and contact Mad Rabbit for a free, a

Mad Rabbit
The numbing
Read more
Recalled Persilux Zebra Blinds
HIGH
CPSC

Persilux Zebra Blinds Recalled for Strangulation Risk, Sold on Amazon

Persilux recalled zebra blinds sold on Amazon after safety hazards were found. The recall cites long operating cords that can cause strangulation and entanglement. The company offers a free repair kit and instructions to remove cords. Consumers should stop using the product immediately and contact Persilux for remedy information.

Persilux
The recalled
Read more
Food & Beverages
HIGH
FDA FOOD

Georgia Nut Co tru fru Freeze-Dried Strawberries Recalled for Metal Fragments (2025)

Georgia Nut Co recalls 170,993 cases of tru fru Dark + White Chocolate Freeze-Dried Strawberries sold nationwide after metal fragments were detected. The recall covers 1.7oz, 3.4oz, and 13oz pouches with UPCs 850048358331, 850048358270, and 850048358379 and distributions to major retailers including Albertsons, CVS, Kroger and Target. Consumers should not eat the product and should await a recall‑

Georgia Nut Co
potential for
Read more
Food & Beverages
HIGH
FDA FOOD

Georgia Nut Co Recalls 76,121 Cases of tru fru Creme Freeze-Dried Strawberries 3.4 oz (2025)

Georgia Nut Co recalls 76,121 cases of tru fru Strawberries + Creme Freeze-Dried Fresh 3.4 oz pouches sold nationwide at retailers including Albertsons, CVS, Food Lion, H-E-B, Kroger, Target, Stew Leonard's and more. A potential for metal fragments in some packages is the hazard. Consumers should stop using the product and contact Georgia Nut Co for a refund or replacement.

Georgia Nut Co
potential for
Read more
Health & Personal Care
HIGH
FDA DEVICE

LeMaitre Vascular Artegraft AG1015 Recall for 1 Unit Over Packing Error (2025)

LeMaitre Vascular recalled 1 Artegraft AG1015 vascular graft distributed to Arkansas hospitals after a packaging size labeling error. The packaging error could lead to using the wrong size graft during surgery. Hospitals and patients should stop using the device and follow recall instructions. See the recall letter for instructions from LeMaitre Vascular or your healthcare provider.

LeMaitre Vascular
The device
Read more
Health & Personal Care
HIGH
FDA DRUG

Aloe Up Sunscreen Lotion SPF 30 Recalled for Microbial Testing Failure in 2025 (11,386 Tubes)

Aloe Up recalled 11,386 tubes of Aloe Up Sport Performance Sunscreen Lotion SPF 30 sold nationwide in the United States. The recall cites cGMP deviations after the product failed total aerobic microbial count testing. Consumers should stop using the product and follow guidance from SV Labs Prescott Corporation or a healthcare provider.

Aloe Up
cGMP deviations:
Read more
Vehicles & Parts
HIGH
NHTSA

Audi S5 Front Seat Belt Retractor Recall Affects 2025 VW Group Vehicles

Audi and Volkswagen Group of America recall 2025 GTI, Golf R, Audi A5, A6 Sportback E-Tron, S5, S6 Sportback E-Tron, 2026 Q4 Sportback E-Tron and Q4 E-Tron vehicles. The torsion bar in the front seat belt retractors may be damaged during production. Dealers will replace one or both front seat belts at no charge. VIN lookups begin Sept 26, 2025 and owner letters go out Nov 21, 2025.

Audi
In a
Read more
Vehicles & Parts
HIGH
NHTSA

AUDI SQ7 Recalled for Fuel Pump Fastener Tightening Issue in 2025 Model

Volkswagen Group of America recalls one 2025 Audi SQ7 over a potential fuel leak from an improperly tightened high pressure fuel pump. The recall affects a single vehicle and is classified as high risk due to fire potential. Owners should contact Volkswagen for inspection and repair at no cost.

AUDI
A fuel
Read more
Health & Personal Care
HIGH
FDA DRUG

Zydus Entacavir Recall 600 Bottles Over Impurity Degradation Issue (2025)

Zydus Lifesciences and Zydus Pharmaceuticals USA recall 600 bottles of Entacavir 1 mg tablets distributed nationwide in the United States. An out-of-specification organic impurity triggered the recall. Stop use immediately and contact a healthcare provider or Zydus for guidance.

Entacavir
Failed impurity/degradation
Read more
Health & Personal Care
HIGH
FDA DRUG

ENTECAVIR Entecavir 0.5 mg Tablets Recalled Nationwide Over Impurity (2025)

Ent ecavir 0.5 mg tablets, distributed nationwide in the United States by Zydus Pharmaceuticals USA Inc., are recalled, affecting 912 bottles. The recall is due to an out-of-specification organic impurity detected in a batch, Class II. Healthcare providers and patients should stop using the product immediately and contact Zydus Pharmaceuticals USA for guidance.

ENTECAVIR
Failed impurity/degradation
Read more
Food & Beverages
HIGH
FDA FOOD

Orwashers Soho Sourdough XL Batard Recalled for Undeclared Sesame Seeds

Orwashers brand Soho Sourdough XL Batard is being recalled after labeling errors could hide sesame seeds. The recall covers 4 pallets of 6 pieces per case in Massachusetts. Consumers should avoid consumption and contact Oven Artisans LLC for refunds or replacements.

Orwashers
Mislabeled: Product
Read more
Food & Beverages
HIGH
FDA FOOD

93,122 Cases of Arctic Shores Frozen Raw Shrimp Recalled Due to Cesium-137 Contamination

Over 93,000 cases of Arctic Shores frozen raw shrimp have been recalled due to potential contamination with Cesium-137. The shrimp were manufactured under insanitary conditions that raise serious health concerns. Consumers should not consume this product and should seek a refund from Great American Seafood Imports.

Arctic Shores
Product manufactured
Read more