adult product Recalls

989 recalls tagged with “adult product”.

Food & Beverages
HIGH
FDA FOOD

Albertsons Store-Made Grilled Chicken & Basil Pasta Extra Large Recalled for Listeria (2025)

Albertsons Companies is recalling store-made Grilled Chicken & Basil Pasta Extra Large sold under Carrs-Safeway, Eagle and Safeway banners. The product contains a bowtie pasta ingredient recalled for Listeria monocytogenes contamination. It was distributed in AK, AR, AZ, CA, CO, HI, LA, NE, NM, NV, OK, SD, TX, UT and WY. Stop using the product and contact Albertsons for refund or replacement.

Albertsons
Listeria monocytogenes.
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Food & Beverages
HIGH
FDA FOOD

Wegmans Recalls 521 Large Ultimate Strawberry Topped Cheesecake Over Undeclared Pecans (2025)

Wegmans Food Markets recalled 521 units of Wegmans Large Ultimate Strawberry Topped Cheesecake distributed in Virginia, Maryland, North Carolina and Washington, D.C. The cake contains undeclared pecans, posing an allergen risk. Consumers should not eat the product and should contact Wegmans for a refund or replacement.

Wegmans Food Markets
Contains undeclared
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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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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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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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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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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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Health & Personal Care
HIGH
FDA DEVICE

BD EpiCenter Recall: 2,050 Units Worldwide Over Unauthorized Access Risk

BD recalled 2,050 units of the EpiCenter Microbiology Data Management System due to unauthorized access to product service credentials. The defect could allow access to confidential data. Stop using affected devices and follow manufacturer guidance for updates or replacement.

Becton Dickinson &
Product service
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Food & Beverages
HIGH
FDA FOOD

Black Sheep Egg Company Recalls 23,400 Dozen Free Range Eggs Over Salmonella Risk (2025)

Black Sheep Egg Company is recalling 23,400 dozen Free Range Grade AA Medium White Eggs sold at retail and wholesale locations in Arkansas and Missouri. The recall centers on potential Salmonella contamination. Consumers should not consume the eggs and should contact Black Sheep Egg Company for refund or replacement information.

Black Sheep Egg Company
Potential Salmonella
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Food & Beverages
HIGH
FDA FOOD

Black Sheep Egg Company Recalls 16,245 Dozen Free Range Eggs (18ct) 2025

Black Sheep Egg Company recalled 16,245 dozen Free Range Grade A Large Brown Eggs sold at retail locations in Arkansas and Missouri, and through wholesale brokers in Mississippi, Texas, California and Indiana. The cartons carry UPC 860010568538. Consumers should not eat these eggs and should contact Black Sheep Egg Company for refunds or replacements.

Black Sheep Egg Company
Potential Salmonella
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Tag Statistics

Total Recalls
989

Related Tags

kitchenimmediate actionstop use immediatelyreturn for refundreplacement availableglassplasticpet relatedfda regulatedcpsc regulatedholiday productoutdoor
    adult product Recalls | RecallRadar