stop use immediately Recalls

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

Health & Personal Care
HIGH
FDA DEVICE

Draeger Recalls Airway Connector Due to Cracking Hazard

Draeger recalled 2,050 units of the ErgoStar CM 60 airway connector on November 10, 2025. The recall follows multiple reports of cracks in the device, posing a risk to mechanically ventilated patients. Healthcare providers and patients should stop using the connector immediately.

Draeger
Multiple complaints
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Health & Personal Care
HIGH
FDA DEVICE

Draeger Recalls Airway Connector Over Cracking Hazard

Draeger recalled 14,420 units of its ErgoStar CM 40 airway connector on November 10, 2025, due to cracks forming in the hose. The recall affects multiple states in the U.S. and several countries worldwide.

Draeger
Multiple complaints
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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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Health & Personal Care
HIGH
FDA DRUG

Actavis Recalls Testosterone Gel Due to Leakage Risk

Actavis Laboratories recalled 15,944 cartons of Testosterone Gel on November 7, 2025. The recall follows a defect in the side-seal of the containers, which may allow product leakage. Consumers must stop using the product immediately and contact their healthcare providers for guidance.

TESTOSTERONE
Defective Container
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Health & Personal Care
HIGH
FDA DEVICE

Da Vinci Surgical Systems Recalled Due to Diagnostic Software Flaw

Intuitive Surgical recalled 219 da Vinci surgical systems on November 7, 2025, due to a software error. This error allowed malfunctioning instrument arms to remain in clinical use, posing a high risk of failure. Healthcare providers and patients must stop using these systems immediately.

Intuitive Surgical
Due to
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Vehicles & Parts
HIGH
NHTSA

Gulf States Toyota Recalls 2025 Camry Hybrid Over Load Capacity Label Inaccuracies

Gulf States Toyota, Inc. recalls 2025 Camry Hybrid vehicles equipped with GST accessories after discovering load carrying capacity labels may display inaccurate added weight values. The mislabeling could cause the vehicle to be overloaded, increasing the risk of a crash. Owners should contact GST for a free label replacement; letters were mailed September 16, 2024.

Gulf States Toyota
A vehicle
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Food & Beverages
HIGH
FDA FOOD

Costco Recalls 142,532 Kirkland Signature Caesar Salad Units Over Plastic Dressing Packet (2025)

Costco Wholesale Corp is recalling 142,532 Kirkland Signature Caesar Salad units sold nationwide after discovering the 3oz sealed Caesar Dressing packet may contain plastic material. The dressing packet inside the salad may contain plastic material. Consumers who bought this product should not eat it and should contact Costco for a refund or replacement.

Costco
The 3oz.
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Health & Personal Care
HIGH
FDA DRUG

Fresenius Kabi Famotidine Injection Recall Expands for Microbial Contamination in 2.2 Million Vials

Fresenius Kabi USA, LLC recalls 2,199,850 vials of Famotidine Injection, U.S. distribution nationwide plus Alaska, Hawaii and Puerto Rico after endotoxin testing concerns. The microbial contamination risk prompted an immediate stop-use order. Healthcare providers and patients should follow recall guidance and seek alternatives through their providers.

Famotidine
Microbial Contamination
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Health & Personal Care
HIGH
FDA DEVICE

Bard Peripheral Vascular Catheter Drainage Tray Recalled Due to Hazard

Bard Peripheral Vascular recalled 1,240 Safe-T-Centesis Catheter Drainage Trays due to safety indicator defects. The recall affects products distributed nationwide since November 6, 2025. The defect may cause serious injuries during use in medical procedures.

Bard Peripheral Vascular
Acute drainage
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Health & Personal Care
HIGH
FDA DEVICE

C.R. Bard Recalls Ureteral Stent Kit Due to Labeling Discrepancy

C.R. Bard recalled 4,350 units of the InLay Optima Ureteral Stent Kit on November 6, 2025. The recall was initiated due to a labeling discrepancy where the actual size of the stent may not match its label. This affects distribution across the U.S. and several countries worldwide.

C.R. Bard
Labeling discrepancy;
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Recalled Umeyda Shortsleeve Nightgown – Baby Pink Stripe
HIGH
CPSC

Umeyda Nightgowns Recalled for Burn Risk in 2025 Sold on Amazon

Umeyda recalled 100% cotton girls' nightgowns sold on Amazon. The recall involves nightgowns with a pocket and a front button closure. The garments do not meet mandatory flammability standards and pose a burn risk. Stop using them and email ameyda123@163.com for a full refund.

Umeyda
The recalled
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Recalled STIHL BR 800 X Magnum Backpack Blower
MEDIUM
CPSC

STIHL BR 800 Magnum Backpack Blowers Recalled for Laceration Hazard (2025)

STIHL is recalling BR 800 Magnum backpack blowers sold through authorized STIHL dealers from May 2025 through September 2025. The recall targets units with serial numbers 546515117 to 547916107. The fan wheel inside the blower can break apart, creating a laceration hazard. Consumers should stop using the recalled units and bring them to an authorized STIHL servicing dealer for a free inspection is

STIHL
The fan
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Recalled Vevor Baby Swing in White/Gray with White Base and Mosquito Net, Model Number BB501
HIGH
CPSC

Sanven Technology Recalls 3 Vevor Baby Swing Models for Suffocation Risk (2025)

Sanven Technology recalls 3 Vevor Baby Swing models on 2025-11-06 for a suffocation risk linked to an incline greater than 10 degrees. The swings carry the VEVOR trademark and are labeled as Multi-Function Electric Swing with model numbers BB501K, BB702A, and BB005. Consumers should stop using the swings immediately and contact Sanven Technology for a full refund.

Sanven Technology
The swings
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