replacement available Recalls

1,215 recalls tagged with “replacement available”.

Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical PERIFIX FX Epidural Set Recalled for Lid-Position Defect in 2025

B Braun Medical recalls the PERIFIX FX Continuous Epidural Anesthesia Set and PERIFIX Tuohy Epidural Needle nationwide after a lid-position defect is identified. The issue involves the lid of the catheter connector being in the incorrect position. Healthcare providers are advised to stop using the device and follow the manufacturer’s recall instructions.

B Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Enterix InSure ONE FIT Recall Affects 201,426 Tests Over False Negatives (2025)

Enterix recalled 201,426 InSure ONE Fecal Immunochemical Test kits after a sensitivity failure linked to Test Card Lot TT241102. The issue may cause false negative results. Healthcare providers and patients should stop using the affected kits and follow the manufacturer’s recall instructions.

Enterix
InSure ONE
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Health & Personal Care
HIGH
FDA DEVICE

Baxter Healthcare Oral Probe Recalled for 5,209 Units Misconfigured as Rectal Probes (2025)

Baxter Healthcare recalled 5,209 oral/axillary probes used with Welch Allyn SureTemp Plus thermometers nationwide in the United States, Canada and Colombia. The probes were inadvertently programmed with the rectal configuration, which can yield a lower temperature reading. Healthcare providers and patients should stop using the affected probes immediately and follow Baxter’s recall instructions.

Baxter Healthcare
Affected oral/axillary
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Food & Beverages
HIGH
FDA FOOD

Lawrence Wholesale Shrimp Cocktail Bowls Recalled for Cs-137 Contamination Risk (2025)

Lawrence Wholesale recalled 8,400 cases of Shrimp Cocktail Bowl products sold to Kroger stores in 15 states on Sept. 16, 2025 due to potential Cesium-137 contamination. The recall involves 7oz and 17oz clear plastic bowls with UPCs 011110622952 and 011110624840. Consumers should not consume the product and should contact Lawrence Wholesale LLC for refund or replacement by email.

Lawrence Wholesale
Product manufactured
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Health & Personal Care
HIGH
FDA DRUG

IntegraDose Oxytocin IV Solution Recall 2025 for Subpotent Drug, 853 Bags Nationwide

IntegraDose Compounding Services recalled 853 IV bags of Oxytocin 30 Units/500 mL in 0.9% sodium chloride. The recall is nationwide in the United States. Testing found no oxytocin in the IV bags. Stop using the product and contact IntegraDose or a healthcare provider for guidance.

IntegraDose Compounding Services
Subpotent Drug:
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Health & Personal Care
HIGH
FDA DEVICE

Alcon CONSTELLATION Ultravit 10K & HyperVit 20K Recall for 28,323 Units (2025)

Alcon recalls 28,323 CONSTELLATION Ultravit 10K and CONSTELLATION HyperVit 20K devices used in hospitals worldwide. The recall lists an unspecified hazard. Hospitals should stop using the devices immediately and follow the manufacturer’s instructions. Access the FDA recall notice for details.

Alcon
XXX
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Health & Personal Care
HIGH
FDA DRUG

Graviti Pharmaceuticals Bupropion Hydrochloride XL 300 mg Recall Impacts 46,512 Bottles (2025)

Graviti Pharmaceuticals Private Limited manufactured Bupropion Hydrochloride Extended-Release Tablets XL 300 mg, distributed nationwide by Rising Pharma Holdings, Inc., in 46,512 bottles. The recall cites failed tablet specifications. Stop using the product immediately and contact the manufacturer or your healthcare provider for guidance.

Bupropion Hydrochloride
Failed Tablet/Capsule
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Health & Personal Care
HIGH
FDA DRUG

Skin MD Body Acne Cleanser Recalled for Elevated Benzene Levels (2025)

Skin MD by Dr Monika Kiripolsky recalled its Body Acne Cleanser after detecting elevated benzene levels. The recall covers products associated with Lot # 58170A and Lot # 58172A distributed in CA and GA. Consumers should stop use and seek guidance from a healthcare provider.

Skin MD
Chemical Contamination:
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Health & Personal Care
HIGH
FDA DRUG

Unique Pharmaceuticals Cetirizine Hydrochloride 10 mg Tablets Recalled Nationwide in 2025

9,936 bottles of Cetirizine Hydrochloride Tablets USP 10 mg were recalled nationwide in the United States. Manufactured by Unique Pharmaceuticals Labs and distributed by Rising Pharma Holdings, the lot carries imprint with the wrong ID. Stop using the product immediately and contact the manufacturer or your healthcare provider for guidance.

Cetirizine Hydrochloride
Tablet/Capsules Imprinted
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Health & Personal Care
HIGH
FDA DEVICE

Argon Medical Devices Recalls 1,821 Option Elite IVC Filters for Dilator Resistance Risk (2025)

Argon Medical Devices recalled 1,821 Option Elite Vena Cava Filter System devices sold to U.S. hospitals and international distributors. The recall cites a dilator resistance issue within the introducer sheath that could slow procedures and injure venous tissue. Healthcare providers and patients should stop using the device immediately and follow the recall instructions.

Argon Medical Devices
Due to
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Health & Personal Care
HIGH
FDA DEVICE

GE Healthcare Recalls 82 Millenium Myosight Dual-Head Gamma Cameras for Cardiac Imaging (2025)

GE HealthCare recalled 82 Millenium Myosight dual-head gamma cameras distributed worldwide. The devices could have been moved without adequate detector mounting support. This could cause a detector fall and life-threatening injury. Hospitals and healthcare providers should stop using the cameras immediately and follow manufacturer recall instructions.

GE Healthcare
GE HealthCare
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Health & Personal Care
HIGH
FDA DEVICE

GE HealthCare Recalls 102 Dual-Head Gamma Cameras for Cardiac Imaging (2025)

GE HealthCare recalled 102 dual-head gamma cameras used for cardiac imaging worldwide after finding that some systems past the End of Guaranteed Service could be moved without adequate detector support. This could place excessive stress on detector mounting mechanisms and may cause a detector to fall, posing life-threatening risk. Hospitals and healthcare providers should stop using the devices IM

GE HealthCare
GE HealthCare
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Health & Personal Care
HIGH
FDA DEVICE

GE HealthCare Optima NX Recall for Detector Fall Risk (1 Unit)

GE HealthCare recalled 1 Optima NX dual-head gamma camera worldwide after detecting potential detector mounting failure if the unit is moved without proper support. The risk could cause a detector fall and life-threatening injury. Hospitals should stop using the device and follow the manufacturer’s recall instructions. Contact GE Medical Systems Israel Functional Imaging for guidance.

GE Medical Systems Israel Functional Imaging
GE HealthCare
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Health & Personal Care
HIGH
FDA DEVICE

UIH Technologies uCT 780 MD CT Scanner Recalled for Cover Interference (2025)

UIH Technologies recalled 2 units of the uCT 780 MD computed tomography system after an FDA enforcement notice Z-0220-2026. A third-party outer cover can become trapped between the patient table and gantry, causing mechanical interference during table movement. Hospitals should stop using the device immediately and await instructions from UIH Technologies LLC or their healthcare provider.

UIH Technologies
Third-party outer
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Health & Personal Care
HIGH
FDA DEVICE

GE Medical Systems Israel Recalls Elscint SPX4 Gamma Camera for Cardiac Imaging

GE Medical Systems Israel is recalling 45 units of the Elscint SPX4 dual-head gamma camera worldwide. The recall cites a risk from transporting or relocating systems past End of Guaranteed Service without adequate detector support. Hospitals and clinics should stop using the device immediately and follow manufacturer instructions.

GE Medical Systems Israel
GE HealthCare
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Health & Personal Care
HIGH
FDA DRUG

Major Pharmaceuticals Chlorpromazine 25 mg Tablets Recalled for Nitrosamine Contamination (1256 Bls,

Major Pharmaceuticals recalled 1,256 blister packs of Chlorpromazine Hydrochloride tablets, 25 mg, sold nationwide in the United States. A CGMP deviation led to the presence of N-Nitroso Desmethyl Chlorpromazine above the recommended intake. Healthcare providers and patients should stop using the product and contact Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories for next-步

Chlorpromazine Hydrochloride
CGMP Deviations:
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Tag Statistics

Total Recalls
1,215

Related Tags

immediate actionstop use immediatelyfda regulatedcpsc regulatedreturn for refundfederal law violationsuffocation riskinfant productadult productelectronicbattery poweredchemical hazard