pet related Recalls

224 recalls tagged with “pet related”.

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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Recalled VEVOR Garment Steamer – side view
HIGH
CPSC

Sanven Technology Recalls VEVOR Garment Steamers for Burn Hazard (2025)

Sanven Technology recalled VEVOR Garment Steamers sold online after a burn hazard was identified. Affected units can leak or spit hot water, and the water tank cap can leak or detach. Consumers should stop using the recalled steamers and request a full refund from Sanven Technology.

Sanven Technology
The steamers
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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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Recalled Powerwall 2 AC Battery System
HIGH
CPSC

Tesla Powerwall 2 Recall for Fire Hazard Affects 2020–2022 Units (2025)

Tesla recalls Powerwall 2 energy storage systems sold through Tesla.com and certified installers nationwide due to fire and burn hazards. The lithium-ion cells can stop functioning during normal use, causing overheating and possibly smoke or flame. Owners should stop using the system and contact Tesla for replacement options.

Tesla
The lithium-ion
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Food & Beverages
HIGH
FDA FOOD

Pacific Seafood Recalls 15,498 Lbs Raw Blackened Shrimp Peeled & Deveined Tail-Off Over Sulfite (202

Pacific Seafood recalled 15,498 pounds of Raw Blackened Shrimp Peeled & Deveined Tail-Off sold refrigerated after undeclared sulfite was detected. The product is a shrimp tray produced in Ecuador and distributed in Alabama, Florida and Massachusetts. Consumers should not eat the product and should contact Pacific Seafood Group for a refund or replacement.

Pacific Seafood
Undeclared Sulfite.
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Front view of Recalled Napei Collapsible Infant Bath Tub
HIGH
CPSC

Napei Infant Bath Tubs Recalled for Button Battery Ingestion Hazard (2025)

Napei recalled its collapsible infant bath tubs sold on Amazon by Sefon Store after discovering the built-in thermometer uses button cell batteries that are accessible to children. The batteries pose a risk of ingestion, which can cause serious injuries or death. Stop using the tub immediately and contact Sefon Store for a free replacement battery compartment.

Napei
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

GET TESTED INTERNATIONAL AB Recalled Gut Microbiome Test Mega (2 Units) Over Premarket Approval Viol

GET TESTED INTERNATIONAL AB recalled 2 Gut Microbiome Test Mega units distributed nationwide in the United States. The recall centers on distribution without premarket approval or clearance. Consumers should stop using the device and contact the manufacturer for instructions. The notice was issued in 2025 and is currently active.

GET TESTED INTERNATIONAL AB
Distribution without
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Health & Personal Care
HIGH
FDA DEVICE

GET TESTED INTERNATIONAL AB Recalled 754 Units of 2 in 1 Trichomonas / Gardnerella Test (2025)

GET TESTED INTERNATIONAL AB recalled 754 units of a 2 in 1 Trichomonas / Gardnerella Test distributed nationwide in the United States after regulators found distribution without premarket approval or clearance. The device was distributed without FDA clearance. Patients and healthcare providers should stop using the test immediately and follow the manufacturer’s recall instructions by contactingGET

GET TESTED INTERNATIONAL AB
Distribution without
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Health & Personal Care
HIGH
FDA DEVICE

GET TESTED INTERNATIONAL AB Drug Test Small (4 Substances) Recall 2025

GET TESTED INTERNATIONAL AB distributed 1 unit nationwide in the United States. The device lacked premarket approval or clearance. Stop using the product immediately and contact GET TESTED INTERNATIONAL AB for instructions.

GET TESTED INTERNATIONAL AB
Distribution without
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Health & Personal Care
HIGH
FDA DEVICE

Olympus HX-400U-30 Recall: 7,803 Endoscopic Ligation Devices Recalled in 2025

Olympus Corporation of the Americas recalled 7,803 HX-400U-30 single‑use ligating devices distributed nationwide in the United States. The ligation loop may fail to release or detach. Hospitals and clinics should stop using the device immediately and follow the recall instructions from Olympus or their healthcare providers.

Olympus
Potential that
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Recalled Crate & Barrel Ana Dining Chairs
MEDIUM
CPSC

Crate & Barrel Recalls Ana Dining Chairs Across 15 SKUs for Fall Hazard (2025)

Crate & Barrel recalled Ana Dining Chairs sold at Crate & Barrel stores and Crateandbarrel.com from January 2021 through January 23, 2025 for a fall hazard. The chair legs can break, posing a fall risk. Stop using the recalled chair and contact Crate & Barrel to obtain a free replacement chair and arrange a free pickup.

Crate & Barrel
The legs
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical Extension Set Recalled for 1,200 Units Over Backflow and Occlusion Risk (2025 Recall

B Braun Medical recalled 1,200 extension sets used with Infusomat Space large-volume pumps distributed worldwide to hospitals and clinics. The recall cites potential backflow from secondary IV containers into primary containers and an inability to prime (occlusion). Healthcare facilities should stop using the devices immediately and follow the recall instructions issued by the manufacturer.

B Braun Medical
Potential for
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