All Product Recalls

Browse through 2,959 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

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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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
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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
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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:
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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
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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
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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
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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
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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
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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
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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
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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
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Health & Personal Care
HIGH
FDA DEVICE

BD Phoenix M50 Recall: 4,283 Systems Worldwide Over Access Risk (2025)

BD recalled 4,283 Phoenix M50 Automated Microbiology Systems worldwide after unauthorized access to product service credentials. The unauthorized actor could access affected products and data. Labs should stop using these devices and follow the recall instructions from BD; contact BD for remediation guidance.

BD
Product service
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Food & Beverages
HIGH
FDA FOOD

Southwind Foods' Tovala-brand Frozen Shrimp Recalled for Cs-137 Contamination (93,122 Cases, 2025)

Southwind Foods LLC, doing business as Great American Seafood Imports, recalled 93,122 cases of Tovala-brand frozen raw phosphate-free shrimp after identifying potential Cesium-137 contamination. The recall expands a prior action and notes insanitary production conditions. Consumers who bought the 5 oz IQF bag with UPC 829944085788 should not eat it and should contact the supplier for refund or re

Southwind Foods LLC dba Great American Seafood Imports
Product manufactured
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