metal Recalls

269 recalls tagged with “metal”.

Vehicles & Parts
HIGH
NHTSA

Ford Recalls 2025 Explorer and Aviator for Trailer Tail Light Failure (25C42)

Ford recalls 2025 Explorer and Aviator vehicles sold through Ford dealers due to a faulty body control module that can prevent trailer tail lights from illuminating. The defect may reduce visibility for other drivers when towing a trailer. Interim letters alert owners starting Oct 13, 2025, with a final remedy anticipated in April 2026. Ford will perform the repairs at no charge and provide the an

Ford
Trailer tail
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Health & Personal Care
HIGH
FDA DEVICE

GE Medical Systems MAC VU360 Recall 29,225 Trunk Cable and Module Holder Units (2025)

GE Medical Systems recalled 29,225 MAC VU360 Acquisition Trunk Cable and Module Holder devices worldwide. The defect can occur when a user inserts the Acquisition Module incorrectly, causing excessive bending and wear of the Acquisition Trunk Cable. A damaged sheath or exposed wires may appear. If a damaged cable is not identified and removed from service, it can overheat. Stop use immediately and

GE Medical Systems
If a
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Health & Personal Care
HIGH
FDA DEVICE

Boston Scientific Pacemaker L231 Recalled; 63,851 Units in 2025

Boston Scientific recalled 63,851 L231 pacemakers worldwide on August 20, 2025. The recall covers the ACCOLADE family and related devices, including PROPONENT, ESSENTIO, ALTRUA 2 DR SL/EL, and VISIONIST and VALITUDE CRT-Ps. The software flaw could prevent Safety Mode from initiating when needed. Stop using the device and contact your healthcare provider for instructions immediately.

Boston Scientific
Software to
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Health & Personal Care
HIGH
FDA DEVICE

Boston Scientific Pacemaker Recall Affects 3,620 Units Worldwide in 2025

Boston Scientific recalls 3,620 pacemakers worldwide including VALITUDE CRT-P EL and ACCOLADE family devices. A software update is intended to prevent initiation of Safety Mode due to high battery impedance. Patients and clinicians should stop using affected devices and await manufacturer instructions.

Boston Scientific
Software to
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Food & Beverages
HIGH
FDA FOOD

Best Yet, Arctic Shores, and Great American Frozen Shrimp Recalled for Cs-137 Contamination (2025)

Best Yet, Arctic Shores, and Great American frozen shrimp were recalled by Southwind Foods LLC dba Great American Seafood Imports Co. The recall cites insanitary production conditions that may have contaminated products with Cesium-137. Consumers who purchased these products should not consume them and should contact the company for refunds or replacements.

Best Yet
Product manufactured
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Health & Personal Care
HIGH
FDA DEVICE

Corneat Vision EverPatch+ 180-Unit Recall for Scleral Patch Dehiscence Risk (2025)

CORNEAT VISION recalled 180 units of EverPatch+ scleral reinforcement patch worldwide after complaints of conjunctival wound dehiscence. The issue can lead to early exposure of the surgical patch. Clinicians and patients should stop using the device immediately and follow the manufacturer recall instructions.

CORNEAT VISION
Reviewed complaints
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Health & Personal Care
HIGH
FDA DEVICE

Maquet Cardiovascular Recalls Heartstring III Proximal Seal System 3.8 mm Occluder (32,867 Units) 0

Maquet Cardiovascular recalls the Heartstring III Proximal Seal System, a 3.8 mm intravascular anastomosis occluder used by hospitals worldwide. Three failure modes have been identified: loading failure, deployment failure, and failure to provide adequate hemostasis. Healthcare facilities should stop using the device immediately and follow manufacturer recall instructions.

Maquet Cardiovascular
Three failure
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Health & Personal Care
HIGH
FDA DEVICE

Maquet Cardiovascular Heartstring III Proximal Seal System Recalled for 168 Units Worldwide (2025)

Maquet Cardiovascular recalled 168 Heartstring III Proximal Seal System intravascular occluders worldwide, including the United States. Three failure modes have been identified: loading the Heartstring Seal, deploying it into the aortotomy, and achieving adequate hemostasis. Healthcare facilities should stop using the device and follow the manufacturer’s recall instructions.

Maquet Cardiovascular
Three failure
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Health & Personal Care
HIGH
FDA DEVICE

Philips Ingenuity CT Brazil 728325 CT System Recalled for 3 Units in 2025

Philips recalled 3 Ingenuity CT Family Brazil systems, Model 728325, distributed worldwide, including the United States. A ball screw misalignment after a replacement may cause the patient support table to descend to the lowest position. Hospitals and clinicians should stop using the device and follow Philips recall instructions.

Philips
The patient
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Health & Personal Care
HIGH
FDA DEVICE

Philips Brilliance CT Systems Recalled for Descent Hazard in 2025 (73 Units)

Philips recalled 73 Brilliance CT systems worldwide after determining a ball screw misalignment could cause the patient couch to descend to the lowermost position. The recall covers Brilliance 16 Power, 728240; Brilliance CT 16 Slice, 728246; and Brilliance CT 6 Slice, 728256. Hospitals and clinics should stop using the devices and follow the manufacturer’s recall instructions immediately.

Philips
The patient
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Food & Beverages
HIGH
FDA FOOD

Baker's Authority Recalls 78 Units of Three Seed Mix for Sesame Allergen (2025)

Baker's Authority LLC recalls 78 units of Three Seed Mix, 5 lb bags, distributed to multiple states. The recall follows labeling errors that fail to list sesame as an ingredient. Consumers who purchased this product should not consume it and should email Baker's Authority LLC for refund or replacement information.

Baker's Authority
Product label
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Health & Personal Care
HIGH
FDA DEVICE

Max Mobility Permobil MX2+ SpeedControl Dial Recalled for 15,834 Units in 2025

Max Mobility LLC recalls Permobil Smart Drive MX2+ SpeedControl Dial MX2-3DCK affecting 15,834 units sold through multiple retailers. A faulty electrical connection between the speed control dial and the wheelchair motor can cause loss of control. Stop using the device immediately and follow recall instructions; contact Max Mobility LLC or your healthcare provider for instructions. This recall was

Max Mobility
Due to
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Health & Personal Care
HIGH
FDA DEVICE

Baxter Continu-Flo Intravascular Set Recalled for Tubing Separation — 14,400 Units in 2025

Baxter Healthcare Corporation issued an urgent medical device recall for one lot of Continu-Flo intravascular solution sets, 14,400 units distributed nationwide in the United States. Customer reports indicate tubing separation. Health care providers and patients should stop using the device immediately and follow recall instructions.

Baxter Healthcare
Baxter Healthcare
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Health & Personal Care
HIGH
FDA DEVICE

Medline Medline Extremity Pack DYNJ45701B Sterile Kit Recall Affects 88 Units (2025)

Medline Industries recalled 88 units of the Sterile Extremity Pack DYNJ45701B after finding that kits labeled as sterile had not undergone sterilization. The affected distribution covered Florida, Maryland, New Jersey and Tennessee. Hospitals and clinics should stop using the kit immediately and follow Medline's recall instructions.

Medline Industries
Convenience kits
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Health & Personal Care
HIGH
FDA DEVICE

SeaSpine Orthopedics Recalled 74 Reef TA Inserter Instruments for Reef Interbody System (2025)

SeaSpine Orthopedics recalled 74 Reef TA Inserter instruments used with the Reef Interbody System, distributed worldwide to hospitals and surgical centers. The inserter may cause difficulty disengaging the implant or improper positioning, prolonging surgery and possibly requiring intraoperative revision. Hospitals and surgeons should stop using the device and follow recall instructions from SeaSpn

SeaSpine Orthopedics
Inserter, used
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Tag Statistics

Total Recalls
269

Related Tags

vehicleelectrical hazardnhtsa regulatedreplacement availablerepair availablestop use immediatelyimmediate actionfederal law violationexplosion riskadult productglassoutdoor