metal Recalls

89 recalls tagged with “metal”.

Food & Beverages
HIGH
FDA FOOD

Trader Joe's Vegetable Fried Rice Recalled for Glass Fragments in 9.9 Million Pounds (2026)

Ajinomoto Foods North America recalled Trader Joe's Vegetable Fried Rice sold at Trader Joe's nationwide after glass fragments were found in the product. The contamination involves glass shards ranging from 1 to 3 cm long and 2 to 4 mm wide. Consumers should not eat this product and should contact Ajinomoto Foods North America for refunds or replacements.

Ajinomoto Foods North America
Foreign objects
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Health & Personal Care
HIGH
FDA DEVICE

Philips Allura Xper FD20/10 Recall Affects 85 Imaging Systems in 2026

Philips recalled 85 Allura Xper FD20/10 imaging systems distributed nationwide and internationally. The devices may fail to initiate X-ray imaging or do so intermittently when using the wired foot switch. Hospitals and clinicians should stop using the device and follow the manufacturer’s recall instructions.

PHILIPS MEDICAL SYSTEMS NEDERLAND
Philips has
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Food & Beverages
HIGH
FDA FOOD

Ajinomoto Green Gyoza Dumplings Recalled for Glass Shards in 537,033 Lbs (2026)

Ajinomoto Foods North America recalls 537,033 pounds of Ajinomoto Green Gyoza Vegetable & Edamame Dumplings sold nationwide after glass fragments were found. Glass pieces range from 1 to 3 cm long and 2 to 4 mm wide. Consumers should not eat the recalled dumplings and should contact Ajinomoto Foods North America for a refund or replacement.

Ajinomoto Foods North America
Foreign objects
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Health & Personal Care
HIGH
FDA DEVICE

Civco Medical Instruments Recalls 21 eTRAX Needle Sensors for Aurora Trackers (2026)

Civco Medical Instruments Co. recalled 21 eTRAX Needle Sensors for Aurora Trackers sold to healthcare providers in Ohio, Pennsylvania and Washington. The devices have an inspection and programming error that can cause the needle tip position to be misidentified on the user interface. Clinicians should stop using the devices immediately and follow recall instructions from Civco.

Civco Medical Instruments Co.
There was
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Health & Personal Care
HIGH
FDA DEVICE

Civco Medical eTRAX 14G Needle Sensor Recall for 5 Units (2026)

Civco Medical Instruments Co. is recalling 5 eTRAX Needle Sensor 14G units for Aurora Trackers. The recall cites a programming and inspection error that could cause the needle tip position to be misidentified on the user interface. Stop using the device immediately and contact Civco for instructions.

Civco Medical Instruments Co.
There was
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Health & Personal Care
HIGH
FDA DEVICE

Olympus SOLTIVE Pro Laser System Recall 2026 — 32 Units Worldwide

Olympus recalled 32 SOLTIVE Pro SuperPulsed Laser System units distributed worldwide after a defect in the 24V power supply may render the device inoperable. The defect can cause smoke or a burning smell, but the issue is contained within the laser console enclosure and self-extinguishing. Stop using the device and follow the manufacturer’s recall instructions.

Olympus
Following a
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Food & Beverages
HIGH
FDA FOOD

Savannah Bee Company Honey BBQ Sauce Mustard Recalled for Soy and Wheat Allergens (2026)

4,611 bottles are recalled nationwide. The product is Savannah Bee Company Honey BBQ Sauce Mustard, distributed to numerous states. The bottle actually contains Honey BBQ Sauce 'Sweet' which contains wheat and soy not declared on the Mustard label. Stop using the product and contact Savannah Bee Company for a refund or replacement.

Savannah Bee Company
Undeclared Allergens:
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Health & Personal Care
HIGH
FDA DEVICE

GE Healthcare SIGNA Premier MRI Systems Recalled Worldwide for Ferrous Fittings Hazard (41 Units, 6)

GE Healthcare recalled 41 SIGNA Premier Whole-Body MRI systems sold worldwide. The devices may have ferrous fittings on the magnet rear instead of brass. If service is performed while the magnet is ramped, the magnetic field could attract the fittings and injure personnel. Hospitals should stop using the devices and follow the manufacturer's recall instructions.

GE Healthcare
Whole-Body MR
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Health & Personal Care
HIGH
FDA DEVICE

Synthes Bone Taps Recall 33-Unit Lot Swap Causes Incorrect Threading (2026)

Synthes bone taps recalled nationwide in the United States after a lot swap affected 33 units sold through multiple retailers. The defect is an incorrect thread caused by a lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8. Healthcare providers should stop using these devices immediately and follow recall instructions from Synthes.

Synthes
A full
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Recall: 93 PKS Cutting Forceps Over Welding Defects (2026)

Olympus Corporation of the Americas recalled 93 PKS Cutting Forceps worldwide due to welding defects that can cause the jaw to break during clinical use. The issue involves Model 3005PK and UDI 00821925036000. Action is required immediately and providers should follow recall instructions.

Olympus Corporation of the Americas
Olympus identified
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Food & Beverages
HIGH
FDA FOOD

Pacific Coast Fresh CO Recalls King Harvest Spinach Hummus 2026 for Aluminum Fragments

Pacific Coast Fresh CO is recalling 239 containers of King Harvest Spinach Hummus sold in Oregon and Washington. Each 10-ounce tub bears UPC 025726311087 and Best By date 2/27/2026. Stop using the product immediately due to aluminum fragments and call Pacific Coast Fresh CO by telephone for refund or replacement.

Pacific Coast Fresh CO
Foreign material
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Food & Beverages
HIGH
FDA FOOD

Pacific Coast Fresh CO Recalls King Harvest Sundried Tomato Hummus Over Aluminum Pieces (2026)

Pacific Coast Fresh CO recalls 348 10-ounce King Harvest Sundried Tomato Hummus containers sold in Oregon and Washington after aluminum pieces were found. The hazard is foreign material aluminum pieces in the hummus. Consumers should not consume the product and should contact Pacific Coast Fresh CO by telephone for refund or replacement.

Pacific Coast Fresh CO
Foreign material
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Food & Beverages
HIGH
FDA FOOD

King Harvest Black Olive Hummus Recalled for Aluminum Pieces in 319 Containers (2026)

King Harvest Black Olive Hummus, sold in 10-ounce plastic tubs and distributed in Oregon and Washington, is recalled after aluminum fragments were found. The recall cites a foreign material hazard. Consumers who purchased it should not consume it and should contact Pacific Coast Fresh CO by telephone for a refund or replacement.

Pacific Coast Fresh CO
Foreign material
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Food & Beverages
HIGH
FDA FOOD

King Harvest Balsamic Hummus Recalled for Aluminum Shards in 326 10oz Tubs (2026)

King Harvest Balsamic Hummus recalled by Pacific Coast Fresh Co. The product was distributed in Oregon and Washington. A foreign material aluminum piece hazard was identified. Consumers should not eat the product and should contact Pacific Coast Fresh Co for refund or replacement information by telephone.

Pacific Coast Fresh CO
Foreign material
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Health & Personal Care
HIGH
FDA DEVICE

Mentor Texas LP Recalls CPX 4 US Breast Tissue Expanders with Suture Tabs (2026)

Mentor Texas LP recalled CPX 4 US Breast Tissue Expanders with Suture Tabs sold worldwide, including US nationwide, after determining infusion sets may contain a dull needle tip. The defect may hinder needle advancement or cause breakage during use. Patients and providers should stop using the device immediately and follow recall instructions from the manufacturer.

Mentor Texas
Infusion sets
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Health & Personal Care
HIGH
FDA DEVICE

Mentor Texas CPX 4 US Breast Tissue Expanders Recall 2026

Mentor Texas, LP recalled CPX 4 US Breast Tissue Expanders with Suture Tabs worldwide on February 18, 2026. The recall covers models SCPX-107MH, SCPX-117MH, SCPX-127MH, SCPX-135MH, SCPX-146MH and SCPX-156MH. Infusion sets may include a dull needle tip that is difficult to advance and may break. Stop using the device and follow recall instructions from the manufacturer, with recall notification by-

Mentor Texas
Infusion sets
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Health & Personal Care
HIGH
FDA DEVICE

Medline Sterile Radiology Procedure Kits Recalled for Sterility Breach (2026)

Medline Industries recalled 420 Sterile Radiology Procedure Kits, Model DYNDH1491B, distributed nationwide in Minnesota after a potential breach in sterile pouch packaging. The defect may compromise product sterility. Stop using the kit immediately and contact Medline or your healthcare provider for instructions.

Medline Industries, LP
There is
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Tag Statistics

Total Recalls
89

Related Tags

glasslaceration riskimmediate actionstop use immediatelyreturn for refundreplacement availablefda regulatedkitchenplasticelectrical hazardcpsc regulatedinfant product