stop use immediately Recalls

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

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
Read more
Health & Personal Care
HIGH
FDA DEVICE

Boston Scientific NephroMax Kit Recall Covers 458 Units Over Foreign Material Migration Risk

Boston Scientific Corp. recalls 458 NephroMax Kit units using Encore 26 Inflation Devices after an internal review found foreign material particles could migrate from the inflation device into balloon dilatation catheters. The recall affects UPNs M0062101180 and M0062101600 worldwide. Healthcare providers should stop using the device immediately and follow manufacturer recall instructions.

Boston Scientific
The Encore
Read more
Health & Personal Care
HIGH
FDA DEVICE

Boston Scientific Encore 26 Inflation Device Recalled Over Foreign Particle Contamination

Boston Scientific recalls 39,739 Encore 26 Inflation Devices worldwide after an internal investigation found foreign material particles could migrate from the device into balloon dilation catheters. The high-severity recall affects interventional cardiology and peripheral interventions devices. Stop using immediately and await recall instructions from Boston Scientific or healthcare providers.

Boston Scientific
The Encore
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips Pinnacle3 Recall: 810 Units Over ROI Image Error in 2025

Philips Medical Systems recalled 810 Pinnacle Radiation Therapy Planning System units nationwide to healthcare providers. A software issue may cause an image error of the Region of Interest for HFP, FFS, and FFP orientations. Hospitals and clinics should stop using the software immediately and follow the manufacturer’s instructions.

Philips Medical Systems
Due to
Read more
Food & Beverages
HIGH
FDA FOOD

M.O.M Enterprises Recalls 85,248 Organic BABY Bedtime Drops Over Spoilage Risk (2025)

M.O.M Enterprises recalled 85,248 units of Organic BABY bedtime drops sold through Multiple Retailers in 31 states. The product is a liquid dietary supplement for infants aged 4 months and older and may spoil due to yeast contamination. Consumers should not consume the product and should seek a refund or replacement from M.O.M Enterprises, LLC.

M.O.M Enterprises
Potential for
Read more
Health & Personal Care
HIGH
FDA DEVICE

Tandem Diabetes Care Recalls 122,958 t:slim X2 and Tandem Mobi Pumps Over Autobolus Risk (2025)

Tandem Diabetes Care recalled 122,958 insulin pumps nationwide in the United States, including Puerto Rico. A software defect in versions 7.9.0.1 and 7.10.1 for the t:slim X2 and version 7.9.0.1 for the Tandem Mobi paired with a Dexcom G7 sensor can trigger an unexpected automatic insulin correction bolus, raising the risk of hypoglycemia. Users should stop using the affected devices and follow a)

Tandem Diabetes Care
A software
Read more
Health & Personal Care
HIGH
FDA DEVICE

Wasatch Photonics Raman Spectrometers Recall Expanded for Laser Safety Risks (2025)

Wasatch Photonics recalled 192 Raman spectrometers in the United States after identifying two potential laser safety failure modes. Models 785-SR-ILP, 785-SR-ILC, 830-SR-ILP, 830-SR-ILC, and 785-ER-ILC are included. The defect could occur under excessive force or extreme continuous vibration. Stop using immediately and follow the manufacturer’s recall instructions.

WASATCH PHOTONICS
Two new
Read more
Health & Personal Care
HIGH
FDA DEVICE

AVID Medical CPT BASIC IR PACK 1646381 Recall for Sterility Risk (2025)

AVID Medical recalls 228 CPT BASIC IR PACKs sold nationwide, including Florida, due to open header bag seals that may compromise sterility. The recall is active as of September 17, 2025. Consumers should stop use and follow manufacturer instructions.

AVID Medical
Potential for
Read more
Health & Personal Care
HIGH
FDA DEVICE

AVID Medical JACK421-04 ENT PACK Recalled for Sterility Risk (2025)

AVID Medical recalled 57 JACK421-04 ENT PACK convenience kits nationwide in Florida. The open header bag seals could compromise sterility. Consumers should stop using the device and follow manufacturer instructions for recall resolution.

AVID Medical
Potential for
Read more
Food & Beverages
HIGH
FDA FOOD

Hans Kissle Company Recalls 66 Units of Red Bliss Potato Salad for Undeclared Wheat (2025)

Hans Kissle Company recalled 66 units of Red Bliss Potato Salad distributed in MA, RI, CT, NJ and NY. The recall is due to undeclared wheat and a mislabeling that identifies the product as potato salad while the unit contains pasta salad. Consumers should not eat the product and should contact Hans Kissle Company for refund or replacement via email.

Hans Kissle Company
Contains undeclared
Read more
Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter DxC 500i Clinical Analyzer Modules Recalled for Processing Delays (2025)

Beckman Coulter has issued a recall for 116 DxC 500 AU Module with ISE and DxC 500i components sold internationally. The recall date is 2025-08-04. A processing fault can cause the Clinical Chemistry test to stay In Progress when an Immunoassay test is run between CC tests. Delays may occur. Stop using the device and contact Beckman Coulter for instructions.

Beckman Coulter
On a
Read more
Recalled Baby Loren Children's Joy Loungewear
HIGH
CPSC

Baby Loren Recalls 4 Morning Loungewear Styles for Burn Risk (2025)

Baby Loren recalls four Morning children’s 100% cotton loungewear dresses in 2025 for fire safety violations. The recall involves dresses with neck labels listing October 2022 or October 2023 and batch numbers ending in 3465, 3585, 3599 or 3569. Consumers should stop using the dresses and contact Baby Loren for a full refund.

Baby Loren
The recalled
Read more
Health & Personal Care
HIGH
FDA DEVICE

Waldemar Link Recall Reaches 8 Units of LinkSymphoKnee Tibial Components Over Uncoated Screws (2025)

Eight modular LinkSymphoKnee TiNbN tibial components are under recall after production with two uncoated security screws. Waldemar Link GmbH & Co. KG disclosed the issue. The devices were distributed worldwide, including CO, IN, NJ and TX in the United States, plus Germany and Italy. Consumers should stop using the device immediately and follow manufacturer instructions.

Waldemar Link GmbH & Co. KG
Some modular
Read more
Recalled KidKraft Farm to Table Play Kitchen
CRITICAL
CPSC

KidKraft Backyard Kids Farm to Table Play Kitchen Recall 2025 After Strangulation Hazard

Backyard Kids recalled KidKraft Farm to Table Play Kitchens in 2025 after one death was reported at multiple retailers. The hazard arises from hooks that hold toy accessories where clothing can snag during climbing or crawling through the back opening. Stop using the play kitchen immediately and contact Backyard Kids for free replacement hooks or repair.

KidKraft
If young
Read more
Previous
12345...108
Next

Tag Statistics

Total Recalls
2,153

Related Tags

immediate actionreplacement availablerepair availablefda regulatedinfant producttoddler productchildren productadult productelderly productworkplacemetalplastic