pet related Recalls

49 recalls tagged with “pet related”.

Health & Personal Care
HIGH
FDA DEVICE

Olympus MAJ-1443/MAJ-1444 Endoscope Suction Valves Recalled in 2026

Olympus Corporation of the Americas recalls 47,383 MAJ-1443 and MAJ-1444 endoscope suction valves distributed nationwide in the United States. The valves are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. Hospitals and clinics should stop using the valves immediately and follow the manufacturer’s recall instructions.

Olympus Corporation of the Americas
The MAJ-1443
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Recalled EnHomee 10 drawer dresser (front)
HIGH
CPSC

EnHomee 10-Drawer Dressers Recalled for Tip-Over Hazard (2026)

EnHomee recalled its 10-Drawer Dressers sold on Amazon after determining tip-over and entrapment hazards. The recall also notes a violation of the STURDY Act mandatory standard. Consumers should stop using unanchored dressers and contact EnHomee for a full refund.

EnHomee
The recalled
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Food & Beverages
HIGH
FDA FOOD

J2C Hawaii Recalls Tiki Bar Candy Due to Allergen Mislabeling

J2C Hawaii recalled Tiki Bar Candy Dark Chocolatey Peanut Butter & Pretzel on January 30, 2026. The recall affects approximately 300 units distributed in Hawaii. The product mislabels peanuts, posing a risk to consumers with peanut allergies.

J2C Hawaii
Ingredients List
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Food & Beverages
HIGH
FDA FOOD

Beacon Promotions Recalls M&Ms Peanut Candies Over Allergen Risk

Beacon Promotions recalled 541 units of repackaged M&Ms Peanut candies on January 26, 2026. The candies contain undeclared allergens including milk, soy, and peanuts. Consumers should stop using the product immediately and seek a refund or replacement.

Beacon Promotions
Undeclared allergens
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Food & Beverages
HIGH
FDA FOOD

Mangalm Mangalm Tops GOLD Lime Pickle Recalled for Erucic Acid Adulteration (2026)

Mangalm LLC recalls 40 cases of Tops GOLD Lime Pickle, 31.74 oz jars, produced in India and distributed to California, Nevada, Oregon, Utah and Washington. The recall follows potential adulteration with erucic acid from mustard oil. Consumers who have purchased the product should not consume it and should contact Mangalm LLC for a refund or replacement via email.

Mangalm
Potential adulteration
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Health & Personal Care
HIGH
FDA DEVICE

I.T.S. Screw System Recalled for MRI Heating Risk in 5,568 Units (2026)

I.T.S. GmbH has recalled 5,568 units of the I.T.S. Screw System sold nationwide in the United States after MRI safety tests showed higher RF-induced temperature increases under some MRI conditions than the IFU outlined. The defect involves MRI RF heating that could burn patients. Patients and healthcare providers should stop using the device immediately and follow the recall instructions.

I.T.S. GmbH
Updated MRI
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Health & Personal Care
HIGH
FDA DRUG

Gold Star Distribution Recalls Excedrin Migraine 2's 25 CT Over Rodent-Contamination Risk (2026)

Gold Star Distribution recalls Excedrin Migraine 2's, 25-count bottles distributed nationwide in the United States. CGMP deviations involve insanitary conditions including rodent exposure in the distribution center. Consumers and healthcare providers should stop using the product immediately and contact Gold Star Distribution or their healthcare provider for guidance.

Gold Star Distribution
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

Carmex Lip Balm Recalled by Gold Star Distribution for 12-Count Jars and Tubes (2026)

Gold Star Distribution Inc. is recalling Carmex lip balm in 12-count jars and 12-count tubes distributed nationwide in the United States. The recall cites CGMP deviations and insanitary conditions at the distribution center, including rodent exposure. Consumers and healthcare providers should stop using the product immediately and contact Gold Star Distribution for guidance.

GOLD STAR DISTRIBUTION
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

Tylenol Recall by Gold Star Distribution Affects 5 SKUs in 2026

Gold Star Distribution is recalling Tylenol products distributed nationwide. The recall concerns CGMP deviations and insanitary conditions at the distributor’s facility. Consumers should stop using these Tylenol products immediately and contact Gold Star Distribution for guidance.

Gold Star Distribution
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

Gold Star Distribution Recalls Vaseline and Other Petroleum Jelly Products for CGMP Violations (2025

Gold Star Distribution is recalling petroleum jelly products nationwide in the United States. The recall covers Vaseline brand products and other jelly variants distributed by Gold Star Distribution. The issue stems from CGMP deviations at the distribution center and insanitary conditions due to rodent exposure. Consumers should stop using the affected products immediately and contact the company.

Gold Star Distribution
CGMP Deviations:
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Food & Beverages
HIGH
FDA FOOD

Gregory's Foods Cookie Dough Recalled for Undeclared Peanuts

Gregory's Foods recalled 308 cases of White Chocolate Macadamia Nut frozen cookie dough on December 19, 2025. The product contains undeclared peanuts, posing a serious allergy risk. Consumers should not consume the product and seek refunds.

Gregory's Foods
Undeclared peanuts.
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Food & Beverages
HIGH
FDA FOOD

Lunds & Byerlys Monster Cookies Recalled Due to Undeclared Allergens

Lunds & Byerlys recalled 1,296 cookies on December 3, 2025, due to undeclared allergens including peanuts, eggs, and soy. The recall affects 108 cases of Monster Cookies sold in Minnesota. Consumers should not eat the product and seek a refund.

Lund Food Holdings
Undeclared allergens
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Food & Beverages
HIGH
FDA FOOD

Mondelez Recalls Ritz Peanut Butter Crackers Over Allergen Risk

Mondelez Global recalled 70 cases of Ritz Peanut Butter Cracker Sandwiches on November 28, 2025. The recall stems from undeclared peanut allergens due to mispackaging. The affected product was distributed in eight states including Alabama and New York.

Mondelez Global
Undeclared allergens
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Food & Beverages
HIGH
FDA FOOD

Imu-Tek Colostrum Powder Recalled Due to Undeclared Allergen

Imu-Tek Animal Health recalled 113 bottles of Immuno-5 Colostrum Powder on November 25, 2025. The product contains an undeclared milk allergen, posing a risk to consumers with milk allergies. The recall affects states including CA, TX, and FL.

Imu-Tek Animal Health
Undeclared milk
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Food & Beverages
HIGH
FDA FOOD

Silvestri Sweets Recalls Cookie Butter Bark Over Pecan Hazard

Silvestri Sweets Inc recalled 37,314 bags of Cookie Butter Holiday Bark on November 21, 2025. The recall stems from undeclared pecan allergens, posing a risk to consumers with nut allergies. The affected product was distributed nationwide through Aldi stores.

Silvestri Sweets Inc dba Carousel Candies
Undeclared pecan
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Food & Beverages
HIGH
FDA FOOD

Taproom Gourmet Snack Mix Recalled Over Undeclared Allergens

Egress Capital Partners recalled 3,547 cases of Taproom Gourmet bulk "Park" Mix on September 18, 2025. The product lacks an ingredient label and contains undeclared allergens including peanuts and almonds. Consumers should not consume the product and seek a refund.

Egress Capital Partners
No ingredient
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Food & Beverages
HIGH
FDA FOOD

Taproom Gourmet Recalls 15lb Broadway Mix Over Allergen Risks

Taproom Gourmet recalled 3,547 cases of its 15lb bulk "Broadway" Mix on September 18, 2025. The product lacks an ingredient label and contains undeclared allergens including peanuts, sesame, wheat, and soy. Consumers should not consume the product and seek refunds.

Taproom Gourmet
No ingredient
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Food & Beverages
HIGH
FDA FOOD

Taproom Gourmet Snack Mix Recalled Due to Allergen Risks

Taproom Gourmet recalled 3,547 cases of its "Fifth Avenue" Mix on September 18, 2025. The product lacks an ingredient label and contains undeclared allergens including peanuts, almonds, cashew, and soy. Consumers in NY, NJ, CT, CA, IL, and FL are urged to avoid consumption.

Taproom Gourmet
No ingredient
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Food & Beverages
HIGH
FDA FOOD

Gina Marie Bakery Recalls Cookies Over Undeclared Ingredients

Gina Marie Bakery recalled 172 cases of Italian Sesame Cookies on September 10, 2025. The recall was initiated due to undeclared sesame and artificial colors. Consumers should not consume these cookies and can seek a refund.

Gina Marie Bakery
Undeclared Sesame,
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Health & Personal Care
HIGH
FDA DEVICE

Philips Ultrasound C9-4 Transducer Recalled for Lifespan Labelling — 1 Unit (2025)

Philips Ultrasound recalled 1 unit of the C9-4 Ultrasound Transducer, Model No. 989605365021, distributed nationwide in the United States. The recall focuses on clarifying and labeling the device’s useful life. Healthcare providers and patients should stop using the device immediately and follow Philips’ instructions for replacement or further steps.

Philips Ultrasound
To provide
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Tag Statistics

Total Recalls
49

Related Tags

fire hazardelectrical hazardchemical hazardsuffocation risktip over riskinfant productadult productcpsc regulatedfda regulatednhtsa regulatedstop use immediatelyreturn for refund