metal Recalls

269 recalls tagged with “metal”.

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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Health & Personal Care
HIGH
FDA DEVICE

GE Healthcare CSCS V3 MAS800 Central Station Recalled for 2,306 Units Worldwide (2025)

GE Healthcare recalled 2,306 CSCS V3 MAS800 Central Station desktops worldwide after identifying a software fault that can trigger a continuous reboot cycle. The issue can result in a loss of central monitoring for connected patients. Hospitals should stop using the affected devices and follow the recall instructions from GE HealthCare and Wipro GE Healthcare Private Ltd.

GE Healthcare
GE HealthCare
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Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems Recalls 32,433 Basic Biopsy Trays Re-Gassed After EO Sterilization (2025)

American Contract Systems recalled 32,433 basic biopsy trays distributed nationwide in the United States. These trays were re-gassed after a nonconformance occurred during the initial Ethylene Oxide gas injection. The trays have not been validated for exposure to multiple sterilization cycles. Healthcare providers and patients should stop using affected trays and follow recall instructions.

American Contract Systems
Identified products
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Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems Recalls 32,433 Medical Convenience Kits Over EO Re-Gassing Risk (2025)

American Contract Systems Inc. recalls 32,433 medical convenience kits distributed nationwide to healthcare facilities in SD, IA, MN, WA, and IL. Re-gassed after a nonconformance occurred during Ethylene Oxide gas injection. The kits have not been validated for multiple sterilization cycles. Healthcare providers should stop using the devices immediately and follow recall instructions.

American Contract Systems
Identified products
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Food & Beverages
HIGH
FDA FOOD

Pacific Coast Producers Fruit Cocktail Recalled for Lead Contamination in 15 oz Cans (609 cases)

Pacific Coast Producers recalled 609 cases of Fruit Cocktail in 15 oz cans distributed by Wegmans Food Markets over lead contamination concerns. The recall cites potential contamination with lead. Consumers who purchased the product should not consume it and should contact Pacific Coast Producers for a refund or replacement.

Pacific Coast Producers
Potential contamination
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Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems Recalled 32,433 Orthopedic Surgical Kits Over Re-Gassing Risk (2025)

American Contract Systems recalled 32,433 medical convenience kits sold through multiple retailers nationwide in SD, IA, MN, WA and IL. The devices were re-gassed after a nonconformance in the Ethylene Oxide sterilization process. The sterilization cycles have not been validated, so quality, safety and effectiveness cannot be confirmed. Consumers and healthcare providers should stop using the kits

American Contract Systems
Identified products
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Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Nederland Recall Expands for Allura Xper FD20/15 OR Table Model 722059 (2025

Philips Medical Systems Nederland B.V. recalls 8 medical tables worldwide due to BIOS battery depletion risk. The recall affects Allura Xper FD20/15 OR Tables with model number 722059. The BIOS battery may deplete faster than expected, causing the system not to start without warning. Hospitals and healthcare providers should stop using the device immediately and follow the recall instructions.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The BIOS
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Health & Personal Care
HIGH
FDA DEVICE

LeMaitre Vascular Artegraft Collagen Vascular Grafts Recall 2025: 28 U.S. Units Affected

LeMaitre Vascular recalled 28 Artegraft Collagen Vascular Grafts distributed nationwide in 17 states. The grafts use bovine carotid arteries sourced from a supplier not reviewed by the appropriate regulatory authority. Patients and healthcare providers should stop using the device immediately and contact LeMaitre Vascular for instructions.

LeMaitre Vascular
The bovine
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Health & Personal Care
HIGH
FDA DEVICE

Getinge 88-Series Washer-Disinfector 88-5 Recalled for Overheat Risk in 788 Units (2025)

Getinge Disinfection Ab recalled 788 units of the 88-Series Washer-Disinfector worldwide, including US states Colorado, Massachusetts, New Mexico and New Hampshire. The device can overheat if circulation pressure calibration is not performed or performed incorrectly and the low-pressure alarm fails to trigger. Manufacturers advise stopping use and following recall instructions.

Getinge Disinfection Ab
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Baxter Healthcare Recalls 136,512 CLEARLINK IV Sets DUO-VENT for Leak Risk (2025)

Baxter Healthcare recalled 136,512 CLEARLINK System Solution Set DUO-VENT IV sets distributed nationwide in the United States after detecting a leak risk. The Luer Activated Valve design may leak, potentially compromising IV administration. Hospitals and patients should stop using the device immediately and follow Baxter recall instructions.

Baxter Healthcare
IV sets
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Health & Personal Care
HIGH
FDA DEVICE

ConvaTec DuoDERM Extra Thin Dressings Recalled in 2025 for Foreign Matter

ConvaTec recalled 80,980 DuoDERM Extra Thin wound dressings distributed nationwide in the United States. The dressings may contain foreign matter, which could compromise wound care. Healthcare providers and patients should stop using the dressings and follow recall instructions.

ConvaTec
Wound dressing
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Health & Personal Care
HIGH
FDA DEVICE

Northeast Scientific NES Reprocessed 1.4mm OTW Turbo Elite Laser Atherectomy Catheter Recall 173 Un­

Northeast Scientific recalled 173 units of the NES Reprocessed 1.4mm OTW Turbo Elite Laser Atherectomy Catheter distributed nationwide to U.S. healthcare facilities. The device is not cleared for marketing in the United States due to sterility concerns. A breach in the sterile barrier packaging could compromise sterility. Health care providers and patients should stop using the device immediately.

Northeast Scientific
Potential for
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Recalled Lulive 12-Drawer Dresser (front)
HIGH
CPSC

Lulive 12-Drawer Dressers Recalled for Tip-Over Risk in 2025

Lulive recalled 12-drawer dressers sold on Amazon after identifying a risk of serious injury or death from tip-over and entrapment. The dressers are white with a metal frame, a wooden top, 12 collapsing fabric drawers, four side pockets and two hooks. They measure about 12 inches by 39 inches by 45 inches and weigh 30 pounds. Consumers should stop using unanchored dressers immediately and contactL

Lulive
The recalled
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Recalled Nimbus Lock Carabiners
HIGH
CPSC

C.A.M.P. Nimbus Lock Carabiners Recalled for Fall Hazard in 2025

Camp USA recalled Nimbus Lock Carabiners sold through various retailers after a safety concern over the automatic closing mechanism. The carabiner's automatic closing mechanism can break and prevent the gate from closing, creating a fall risk. Stop using the recalled carabiners immediately and contact CAMP for inspection, repair or replacement.

Nimbus
The carabiner's
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Health & Personal Care
HIGH
FDA DEVICE

Siemens MAGNETOM Vida MRI Recall 237 Units Worldwide Over Ice Blockage Risk (2025)

Siemens Medical Solutions USA recalled 237 MAGNETOM Vida MRI scanners sold worldwide to healthcare providers. The recall cites ice forming in the magnet venting system. A quench could lead to a helium leak into the scanning room. Hospitals must stop using the devices and await manufacturer instructions.

Siemens Medical Solutions USA
There is
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Health & Personal Care
HIGH
FDA DEVICE

Siemens MAGNETOM Skyra fit MRI Recalled for Ice Blockage Risk in 30 Units (2025)

Siemens Medical Solutions USA recalled 30 MAGNETOM Skyra fit MRI units worldwide after identifying an ice blockage in the magnet venting system. The defect could prevent helium venting during a quench, causing pressure buildup that may rupture the helium containment and leak into the scanning room. Hospitals should stop using the affected devices immediately and follow the manufacturer’s recall,咨询

Siemens Medical Solutions USA
There is
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Vehicles & Parts
HIGH
NHTSA

Hyundai Recalls 2025-2026 Santa Fe and Tucson for Engine Fastener Issue

Hyundai Motor America is recalling certain 2025-2026 Tucson and Santa Fe vehicles. The connecting rod bolts may have been improperly tightened, which can cause a loss of drive power and engine damage, potentially resulting in an oil leak. Owner notification letters are expected to be mailed October 24, 2025, and dealers will replace the engine free of charge.

Hyundai
A loss
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Food & Beverages
HIGH
FDA FOOD

Country Eggs Shell Egg Recall Affects 81,542 Dozen Across CA and NV

Country Eggs LLC recalled 81,542 dozen shell eggs distributed to 11 consignees in California and Nevada due to potential salmonella contamination. The recall covers Nagatoshi, Nijiya, Mizuho, and Sunshine yolk varieties sold in large AA Brown egg cartons. Consumers should not eat these eggs and should seek refund or replacement.

Country Eggs
Shell egg
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Tag Statistics

Total Recalls
269

Related Tags

electronicimmediate actionstop use immediatelyreturn for refundreplacement availablecpsc regulatedfda regulatedinfant productadult productpet relatedworkplacebattery powered