immediate action Recalls

2,756 recalls tagged with “immediate action”.

Health & Personal Care
HIGH
FDA DEVICE

Northeast Scientific NES Turbo Elite Laser Atherectomy Catheter Recall: 199 Units (2025)

Northeast Scientific recalled 199 units of the NES Reprocessed 2.0mm OTW Turbo Elite Laser Atherectomy Catheter. The device is not cleared for marketing in the United States. Distribution covered 17 states nationwide, including CA, FL, IL, KS, LA, MD, MI, MO, NC, NJ, NM, NV, NY, PA, TN, TX, and VA. Healthcare providers were advised to stop use immediately.

Northeast Scientific
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Baxter Healthcare CLEARLINK CONTIN-FLO IV Solution Sets Recalled for Leaks (2025)

Baxter Healthcare recalled 1,167,120 CLEARLINK CONTIN-FLO IV Solution Sets nationwide after determining they may leak. The non-vented sets include three CLEARLINK Luer Activated Valves and a backcheck valve. Healthcare providers and patients should stop using these devices immediately and contact Baxter for instructions.

Baxter Healthcare
IV sets
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Health & Personal Care
HIGH
FDA DEVICE

Northeast Scientific Laser Atherectomy Catheter Recalled for Sterile Barrier Breach Risk (2025)

Northeast Scientific recalled 165 units of the NES Reprocessed 1.7mm OTW Turbo Elite Laser Atherectomy Catheter sold nationwide in the United States. The recall cites the potential breach of sterile barrier packaging that could compromise sterility. The device is not cleared for marketing in the U.S. and has a high-risk hazard designation. Patients and healthcare providers should stop using the产品,

Northeast Scientific
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Baxter Healthcare CLEARLINK CONTINU-FLO IV Set Recalled for Leaks in 2025 (958,351 Units)

Baxter Healthcare Corporation recalled 958,351 CLEARLINK CONTINU-FLO IV sets due to a leak risk. The non-vented sets feature three Luer activated valves and a Backcheck Valve. Distribution covered nationwide in the United States. Healthcare providers and patients should stop using the device immediately and follow recall instructions on the recall notice.

Baxter Healthcare
IV sets
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Health & Personal Care
HIGH
FDA DEVICE

Baxter Healthcare Recalls 18,720 CLEARLINK Non-DEHP IV Sets for Leakage Risk (2025)

Baxter Healthcare Corp. is recalling 18,720 CLEARLINK System Non-DEHP Conti-Flo Soln Sets sold nationwide in the United States. The IV sets may leak, potentially compromising therapy. Patients and healthcare providers should stop using the device immediately and contact Baxter Healthcare for instructions.

Baxter Healthcare
IV sets
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Health & Personal Care
HIGH
FDA DEVICE

Baxter recalls 2,304 CLEARLINK IV Extension Sets for leak risk in 2025

Baxter Healthcare recalled 2,304 CLEARLINK System Extension Sets distributed nationwide in the United States. The IV extension set may leak, creating a risk to patients. Stop using the device immediately and follow recall instructions from Baxter or your healthcare provider.

Baxter Healthcare
IV sets
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Health & Personal Care
HIGH
FDA DEVICE

Baxter Healthcare Recalls 8,368 CLEARLINK CONTINU-FLO IV Sets for Leakage Risk (2025)

Baxter Healthcare recalled 8,368 CLEARLINK SYSTEM CONTINU-FLO IV sets nationwide after reports the devices may leak. The non-vented sets include a 0.2-micron filter, three CLEARLINK luer activated valves and a backcheck valve, and measure 102 inches in length. Hospitals and clinicians should stop using these units immediately and follow Baxter's recall instructions.

Baxter Healthcare
IV sets
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Health & Personal Care
HIGH
FDA DEVICE

Northeast Scientific NES Reprocessed 2.0mm RX Turbo Elite Laser Atherectomy Catheter Recall 2026

Northeast Scientific recalled 141 units of the NES Reprocessed 2.0mm RX Turbo Elite Laser Atherectomy Catheter nationwide in the United States. The device may have breaches in the sterile barrier packaging that could compromise sterility. Hospitals and patients should stop using the device immediately and await instructions from Northeast Scientific Inc. or their clinicians.

Northeast Scientific
Potential for
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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

NES Reprocessed 1.7mm RX Turbo Elite Laser Atherectomy Catheter Recall: 616 Units In US Distribution

Northeast Scientific Inc. has issued a recall for 616 units of the NES Reprocessed Turbo-Elite Laser Atherectomy Catheter, Model R-417-156. The FDA-listed recall cites breaches in sterile barrier packaging that could compromise sterility. The devices were distributed nationwide in the United States to CA, FL, IL, KS, LA, MD, MI, MO, NC, NJ, NM, NV, NY, PA, TN, TX, and VA. Patients should not be in

Northeast Scientific
Potential for
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Food & Beverages
HIGH
FDA FOOD

Rolling Pin Baking Company Recalls 127,680 Dubai Style Chocolate Pouches for Undeclared Wheat (2025)

Rolling Pin Baking Company LLC is recalling 127,680 Dubai Style Chocolate pouches sold through multiple retailers. The recall was announced on Aug. 29, 2025. The product does not declare wheat in the allergen statement. Consumers should not consume the product and contact the company by email for refund or replacement.

Rolling Pin Baking Company
Product does
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Health & Personal Care
HIGH
FDA DEVICE

Fresenius Medical Care Optiflux Dialyzers Recalled for Press-On Cap Issue (172,494,732 units, 2025)

Fresenius Medical Care recalls 172,494,732 Optiflux High Flux E-beam Dialyzers distributed nationwide in the United States. Caps on these dialyzers were changed from threaded to press-on versions, requiring users to press the caps firmly to secure them. Patients and healthcare providers should stop using these devices immediately and follow recall instructions issued by the manufacturer.

Fresenius Medical Care Holdings
To provide
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Health & Personal Care
HIGH
FDA DEVICE

Northeast Scientific Recalled 561 Units of NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy C

Northeast Scientific recalled 561 units of NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy Catheter. The recall covers all lots within shelf life ending before August 29, 2026. The hazard is breaches in sterile barrier packaging that could compromise sterility. Stop using the device and follow manufacturer instructions for return or replacement.

Northeast Scientific
Potential for
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Tag Statistics

Total Recalls
2,756

Related Tags

stop use immediatelyfda regulatedfederal law violationreturn for refundelectrical hazardchemical hazardinfant productadult productsuffocation risktip over riskfire hazardcpsc regulated