replacement available Recalls

280 recalls tagged with “replacement available”.

Health & Personal Care
CRITICAL
FDA DEVICE

Philips Respironics Trilogy Evo Universal Ventilator Recall Affects 113,717 Units Worldwide in 2026

Philips Respironics recalled 113,717 Trilogy Evo Universal ventilators worldwide on March 2, 2026. The recall cites a condition where using non-pneumatic nebulizers may cause a discrepancy between the set tidal volume and the delivered tidal volume. Patients and caregivers should stop using the device immediately and contact Philips Respironics or their healthcare provider for instructions.

Philips Respironics
Using non-pneumatic
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Health & Personal Care
HIGH
FDA DEVICE

Philips Respironics Trilogy Evo Ventilator Recall 2026 Affects 113,717 Units

Philips Respironics recalled 113,717 Trilogy Evo home-use ventilators worldwide after finding the Obstruction Alarm may fail to trigger, potentially delaying alerts by up to four breaths. The devices were distributed nationwide in the United States and internationally. Consumers should stop using the device immediately and follow the manufacturer’s recall instructions.

Philips Respironics
In some
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Health & Personal Care
HIGH
FDA DEVICE

Civco Medical Instruments Recalls 2 eTRAX 12G Starter Kits for Aurora Trackers (2026)

Civco Medical Instruments recalled 2 eTRAX Needle System Starter Kit 12G units for Aurora Trackers sold to healthcare providers in Ohio, Pennsylvania and Washington. The defect can cause the needle tip position to be incorrectly identified on the user interface. Stop using the device immediately and follow the recall instructions from Civco or your healthcare provider.

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

Philips Respironics Trilogy EV300 Ventilator Recall Affects 113,717 Units in 2026

Philips Respironics recalled 113,717 Trilogy EV300 ventilators sold in the United States and internationally after determining the Obstruction Alarm may fail to trigger within required standards. The alarm can delay alerting caregivers for up to four breaths. Patients and healthcare providers should stop using the device immediately and follow recall instructions from Philips or their clinician.

Philips Respironics
In some
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Health & Personal Care
HIGH
FDA DEVICE

Philips Respironics Trilogy Evo Ventilators Recalled for Tidal-Volume Mismatch (113,717 Units, 2026)

Philips Respironics recalled 113,717 Trilogy Evo ventilators worldwide on March 2, 2026. The recall concerns software Version 1.05.15.00 and the use of non-pneumatic nebulizers with the Trilogy Evo platform. Hospitals and patients should stop using the device immediately and follow recall instructions from Philips Respironics or their healthcare provider.

Philips Respironics
Using non-pneumatic
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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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Food & Beverages
HIGH
FDA FOOD

TG Foods Divided Sunset Multi Collagen Peptides 8 oz Recalled in 2026 Affects 7,980 Units

TG Foods recalled 7,980 units of Divided Sunset Multi Collagen Peptides 8 oz stand-up pouches distributed nationwide. The recall notes the ingredient statement lists wild caught marine collagen and eggshell membrane collagen but does not declare EGG or the specific fish species. Consumers should not consume the product and should contact TG Foods for refund or replacement information.

TG Foods
The product
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Food & Beverages
HIGH
FDA FOOD

American Laboratories Recalls 370 kg Pepsin 1:10,000 Powder Over Salmonella Risk (2026)

American Laboratories recalled 370 kg of Pepsin 1:10,000 Powder sold through 11 wholesale accounts in AZ, CA, FL, MO, NM, OH, SC, UT, WI and one account in Australia after a potential Salmonella contamination. The product carries a possible Salmonella contamination risk. Consumers should not consume the product and should contact American Laboratories for refund or replacement via email.

American Laboratories
Potential Salmonella
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Food & Beverages
HIGH
FDA FOOD

American Laboratories Pepsin Full Strength Powder Recalled for Salmonella Contamination (400 kg, 202

American Laboratories recalled 400 kg of Pepsin Full Strength Powder sold to 11 direct wholesale accounts in AZ, CA, FL, MO, NM, OH, SC, UT, WI and one wholesale account in Australia after a recall cited potential Salmonella contamination. The product is Item #5000545 and packed in double poly-lined drums or boxes. Consumers should not consume this product and should contact American Laboratories,

American Laboratories
Potential Salmonella
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Health & Personal Care
HIGH
FDA DRUG

Macleods Pharma USA Recalls 1,315 Levothyroxine 150 mcg Tablets (2026)

Macleods Pharma USA, Inc. recalls 1,315 bottles of Levothyroxine Sodium Tablets USP 150 mcg distributed nationwide. The drug is subpotent, which may not provide the full therapeutic dose. Stop using and contact your healthcare provider or Macleods Pharma USA, Inc. for guidance.

LEVOTHYROXINE SODIUM
Subpotent Drug
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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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Health & Personal Care
HIGH
FDA DEVICE

Olympus PKS Cutting Forceps 920005PK Recalled for Jaw Break Risk (2026)

Olympus Corporation of the Americas recalled 326 PKS Cutting Forceps worldwide. The devices may have welding defects that cause the jaw to break during use. Stop using the device immediately and follow the recall instructions provided by Olympus.

Olympus Corporation of the Americas
Olympus identified
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Everest Bipolar Cutting Forceps 3005 Recalled for Jaw Break Risk in 2026

Olympus Corporation of the Americas is recalling 106 Everest Bipolar Cutting Forceps worldwide. The devices can have welding defects that may cause the jaw to break during use. Stop using immediately and contact Olympus or your healthcare provider for instructions.

Olympus Corporation of the Americas
Olympus identified
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Health & Personal Care
HIGH
FDA DEVICE

Olympus PK Cutting Forceps Recall 444 Units Worldwide Over Welding Defect (2026)

Olympus Corporation of the Americas is recalling 444 PK-CF0533 cutting forceps distributed worldwide. The devices may have welding defects that can cause the jaw to break during surgery. Stop using the device and follow recall instructions from Olympus or your healthcare provider.

Olympus Corporation of the Americas
Olympus identified
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Health & Personal Care
HIGH
FDA DEVICE

Olympus HALO PKS Cutting Forceps HACF0533 Recalled for Jaw Breakage; 2,648 Units Worldwide (2026)

Olympus Corporation of the Americas is recalling 2,648 HALO PKS Cutting Forceps HACF0533 sold to hospitals and clinics worldwide. The jaw can break during surgical use due to a supplier welding-validation issue. Healthcare facilities should stop using the device immediately and follow Olympus recall instructions for disposition.

Olympus Corporation of the Americas
Olympus identified
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Tag Statistics

Total Recalls
280

Related Tags

immediate actionstop use immediatelyfda regulatedcpsc regulatedelectronicbattery poweredelectrical hazardreturn for refundinfant productadult productmandatory standard violationnhtsa regulated