Health & Personal Care
HIGH
FDA DRUG
Teva Metoprolol Succinate ER 100 mg Recall Expanded for Failed Dissolution Specifications (2026)
METOPROLOL SUCCINATE
Failed Dissolution
stop use immediately Recalls
2,229 recalls tagged with “stop use immediately”.
Health & Personal Care
HIGH
FDA DEVICE
23,568 Medline Surgical Drapes Recalled Over Infection Risk
Medline Industries, LP
Fabric may
Health & Personal Care
HIGH
FDA DEVICE
Ultradent Products Recalls 2,508 Jiffy Original Composite Polisher Cups (Coarse) 12pk (2026)
Composite polisher cups may crumble and break apart easily, which could cause a delay in patient treatment.
Ultradent Products
Composite polisher
Health & Personal Care
HIGH
FDA DEVICE
Medline Medcrest Surgical Gowns Recalled 104,004 Units for Delamination Risk (2026)
Medline Industries
Fabric may
Health & Personal Care
HIGH
FDA DEVICE
Lutronic CLARITY II Laser System Recalled for 1,525 Units Worldwide in 2026
Reports of devices sparking/popping and potentially burning patients.
Lutronic
Reports of
Health & Personal Care
HIGH
FDA DEVICE
BD 10 mL Luer-Lok Syringe Recalled Over Bundle Packaging Mix-Up in US; 204,000 Units Affected
During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.
Becton Dickinson
During the
Health & Personal Care
HIGH
FDA DEVICE
Abiomed Impella RP Flex Recall 4,496 Devices Worldwide Over Sensor Drift (2026)
Abiomed recalled 4,496 Impella RP Flex with SmartAssist devices. The recall cites a differential pressure sensor that may malfunction and drift readings. Stop using the device immediately and follow the manufacturer's recall instructions.
Abiomed
Differential pressure
Health & Personal Care
HIGH
FDA DEVICE
Abiomed Impella RP Recall 179 Units for Sensor Drift Risk (2026)
Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift.
Abiomed
Differential pressure
Health & Personal Care
HIGH
FDA DEVICE
Abiomed Impella RP with SmartAssist Recall Affects 291 Units Worldwide in 2026
Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift.
Abiomed
Differential pressure
Health & Personal Care
HIGH
FDA DRUG
Asteria Health Recalls Testosterone Pellets Due to Metal Contamination
Presence of Foreign substance - potential presence of metal particulate matter
F.H. INVESTMENTS, Inc.
Presence of
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Recalls Azurion 3 M12 Due to Hazard
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Under certain
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Recalls Azurion 7 B12 Table Due to Safety Risk
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Under certain
Health & Personal Care
HIGH
FDA DRUG
Asteria Health Recalls Estradiol Pellets Due to Metal Contamination
Presence of Foreign substance - potential presence of metal particulate matter
F.H. INVESTMENTS, Inc.
Presence of
Health & Personal Care
HIGH
FDA DRUG
Asteria Health Recalls Testosterone Pellets Over Metal Contamination Risk
Presence of Foreign substance - potential presence of metal particulate matter
F.H. INVESTMENTS, Inc.
Presence of
Health & Personal Care
HIGH
FDA DRUG
Asteria Health Recalls Testosterone Pellets Over Metal Contamination
Asteria Health recalled 89,074 testosterone pellets on January 26, 2026. The recall stems from potential metal particulate contamination. Consumers must stop using the product and contact their healthcare provider immediately.
F.H. INVESTMENTS, Inc.
Presence of
Health & Personal Care
HIGH
FDA DRUG
Asteria Health Recalling Estradiol Pellets Due to Metal Contamination
Presence of Foreign substance - potential presence of metal particulate matter
F.H. INVESTMENTS, Inc.
Presence of
Health & Personal Care
HIGH
FDA DRUG
Radnostix SODIUM IODIDE I-131 Solution Recalled for Particulate Matter in 16 Units (2026)
Presence of Particulate Matter: Due to production issues
SODIUM IODIDE I-131
Presence of
Health & Personal Care
HIGH
FDA DRUG
Asteria Health Recalls Estradiol Pellets Over Metal Contamination
Asteria Health recalled 24,099 Estradiol, 10 mg pellets on January 26, 2026, due to potential metal particulate contamination. Consumers should stop using the product immediately. The recall affects pellets distributed nationwide in the USA.
F.H. INVESTMENTS, Inc.
Presence of
Health & Personal Care
HIGH
FDA DRUG
Granules Pharmaceuticals Recalls Trazodone Hydrochloride Over Contamination Risk
Presence of Foreign Tablets/Capsules
TRAZODONE HYDROCHLORIDE
Presence of
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Recalls Azurion 5 M12 Over Safety Risk
Philips Medical Systems recalled 326 Azurion 5 M12 systems on January 26, 2026. The table may move unexpectedly when the Reset Geometry button is pressed, posing a risk to patients and healthcare providers. Immediate cessation of use is advised.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Under certain
Tag Statistics
Total Recalls
2,229