chemical hazard Recalls

1,003 recalls tagged with “chemical hazard”.

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

Northeast Scientific Recalled 1,019 Reprocessed Turbo Elite Atherectomy Catheters Over Sterility Bre

Northeast Scientific Corp. recalled 1,019 units of the NES Reprocessed 1.4mm RX Turbo Elite Laser Atherectomy Catheter. The model is not cleared for marketing in the United States. The recall cites potential breaches in sterile barrier packaging that could compromise sterility. Patients and healthcare providers should stop using the device immediately. Follow the manufacturer's recall instructions

Northeast Scientific
Potential for
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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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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

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

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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Health & Personal Care
HIGH
FDA DRUG

Granules Pharmaceuticals Amphetamine Capsules Recalled for Impurities Degradation Standards (2025)

Granules Pharmaceuticals recalled 9,917 bottles of mixed-salts amphetamine extended-release capsules nationwide. The recall was issued August 28, 2025 and remains active. The FDA cited failed impurities/degradation specifications as the reason. Healthcare providers and consumers should stop using the product immediately and contact Granules Pharmaceuticals for guidance.

Granules Pharmaceuticals
Failed Impurities/Degradation
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Health & Personal Care
HIGH
FDA DRUG

Granules Pharmaceuticals Recall: 11,928 Bottles of Dextroamphetamine Mixed Salts Suspended for Impur

Granules Pharmaceuticals recalled 11,928 bottles of an extended-release amphetamine product. The recall date is 2025-08-28 for Dextroamphetamine saccharate and related salts. The FDA lists the reason as failed impurities and degradation specifications. The recall remains active as of 2025-10-01. Health care providers and patients should stop use and contact the manufacturer for guidance.

Granules Pharmaceuticals
Failed Impurities/Degradation
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Health & Personal Care
HIGH
FDA DRUG

Granules Pharmaceuticals Recalls 3,384 Bottles of Dextroamphetamine ER Capsules for Impurity Issues

Granules Pharmaceuticals Inc. recalls 3,384 bottles of Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate Extended-Release Capsules, 5 mg, 100 capsules per bottle, NDC 70010-029-01, Lot GPC250158A, Exp 06-22-2027. The recall concerns failed impurities/degradation specifications. Healthcare providers and consumers should stop using the

Granules Pharmaceuticals
Failed Impurities/Degradation
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Health & Personal Care
HIGH
FDA DRUG

Ascend Laboratories Recalls ARIPIPRAZOLE 10 mg Tablets Over Superpotent Drug Risks (2025)

Ascend Laboratories, LLC recalls 2,256 bottles of ARIPIPRAZOLE 10 mg tablets distributed nationwide after discovering the product to be superpotent. The recall involves ARIPIPRAZOLE tablets manufactured by Alken Laboratories Ltd. in India and distributed in the United States. The recall date is August 28, 2025, with consumer notification by letter and guidance to stop use.

ARIPIPRAZOLE
Superpotent drug
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Health & Personal Care
HIGH
FDA DRUG

Granules Pharmaceuticals Amphetamine Salts Recall Over Impurities Degradation Specifications (2025)

Granules Pharmaceuticals recalled 11,895 bottles of an extended-release amphetamine product due to failed impurities and degradation specifications. The recall is active nationwide in the United States. The FDA notice lists a high hazard level and urges stop-use and contact with the company or a healthcare provider.

Dextroamphetamine Saccharate
Failed Impurities/Degradation
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Health & Personal Care
HIGH
FDA DEVICE

Siemens MAGNETOM Verio MRI Recalled Globally Over Ice Blockage Risk in Venting System

Siemens Medical Solutions USA recalls 69 MAGNETOM Verio MRIs worldwide after an ice blockage could trap helium gas during a quench. A rupture of the helium containment system may leak helium into the scanning room. The recall affects models with number 10276755 and serials including 40649 and others. Patients and providers should stop using the device and follow manufacturer instructions.

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

Siemens MAGNETOM Skyra MRI System Recall Covers 182 Units Over Ice Blockage Risk

Siemens Medical Solutions USA recalled 182 MAGNETOM Skyra MRI systems worldwide on August 28, 2025. The recall follows a potential ice blockage in the magnet venting system that could cause a helium leak during a quench. Hospitals should stop using affected devices and follow manufacturer instructions for remediation.

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

Siemens MAGNETOM Spectra MRI Recalled, Ice Blockage in Venting May Cause Helium Leak (2025)

Siemens Medical Solutions USA recalls MAGNETOM Spectra MRI with Model Number 10655588 after possible ice blockage in the magnet venting system could cause a helium leak during a quench. The recall covers worldwide distribution including the United States. Patients should stop using the device and follow manufacturer instructions for recall procedures.

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

Siemens MAGNETOM Connectom.X MRI Recalled Globally Over Ice Blockage in Vent System

Siemens Medical Solutions USA issued a global recall for the MAGNETOM Connectom.X MRI system, Model 11371480. One unit is affected. A potential ice blockage in the magnet venting system could cause a helium leak during a quench. Users should stop using the device and await manufacturer instructions.

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

Green Lumber Natural Fuel For Men Capsules Recalled for Tadalafil Contamination

Green Lumber Holdings recalled its Natural Fuel For Men capsules on August 28, 2025. The FDA found the capsules contain tadalafil, a prescription ingredient not approved for this product. Consumers should stop using the product immediately and seek guidance from healthcare providers.

Green Lumber Holdings
Marketed without
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Health & Personal Care
HIGH
FDA DEVICE

Siemens Medical MAGNETOM Vida Fit MRI Recall: 27 Units at Risk of Helium Leak

Siemens Medical recalled 27 MAGNETOM Vida Fit MRI systems after a potential helium containment rupture was identified. Ice blockage in the magnet venting system may prevent helium from escaping, leading to a dangerous pressure build-up. Patients and healthcare providers must stop using the device immediately and follow the manufacturer's instructions.

Siemens Medical Solutions USA
There is
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Tag Statistics

Total Recalls
1,003

Related Tags

immediate actionstop use immediatelyreplacement availablereturn for refundcpsc regulatedfda regulatedelectrical hazardinfant producttoddler productadult productelderly productback to school