Health & Personal Care
HIGH
Drug Recalls Center
2,090 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.
2,090
Total Drug Recalls
24
High Risk Medications
FDA
Official Source
Important Medication Safety Information
- Do not stop taking prescribed medications without consulting your healthcare provider
- Contact your pharmacist or doctor if you have a recalled medication
- Check lot numbers carefully - not all batches may be affected
- Return recalled medications to your pharmacy for proper disposal
Looking for a specific drug? Use the search page to find recalls by medication name, manufacturer, or NDC number.
Read more
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Recalls Allura Xper FD20 Over Electrical Hazard
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips has
Health & Personal Care
HIGH
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical System Recall Over Electrical Hazard Risk
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Broselow Recall Due to Dangerous Dosing Errors in ALS Organizer
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
SunMed Holdings
Product contains
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Recalls Allura Xper FD20 Over Electrical Hazard
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips has
Health & Personal Care
HIGH
FDA DEVICE
ICU Medical Recalls Plum Duo Infusion Pump Over High Hazard Risk
ICU Medical recalled the Plum Duo Infusion Pump on December 15, 2025, after reports of malfunctioning flush programming. The recall affects models 400020401 and 400021001 sold worldwide. This issue may pose a high risk to patient safety.
ICU Medical
Plum Solo
Health & Personal Care
HIGH
FDA DEVICE
Philips Recalls Allura Xper FD10C Systems Over Electrical Hazard
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Recalls Allura Xper FD20 Biplane Over Electrical Hazard
Philips Medical Systems recalled 23 units of the Allura Xper FD20 Biplane on December 15, 2025. The recall affects systems with improperly installed drip trays, posing an electrical hazard. Health providers and patients must stop using the device immediately.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Philips Recalls Allura Xper FD20 OR Table Due to Electrical Hazard
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Issues Recall for Allura Xper FD10/10
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Recalls Allura Xper FD20/20 Over Electrical Hazard
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Philips Recalls Allura Xper FD20 Over Electrical Hazard
Philips recalled 79 Allura Xper FD20 systems on December 15, 2025. The recall affects systems with an improperly installed drip tray which can cause electrical short-circuits. Healthcare providers and patients must stop using the device immediately.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Broselow Pediatric Emergency Tape Recalled Over Dosing Errors
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
SunMed Holdings
Product contains
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Recalls Allura Xper FD20/10 Over Electrical Hazard
Philips Medical Systems recalled four Allura Xper FD20/10 systems on December 15, 2025. The company identified that a drip tray was not installed, posing a risk of electrical shorts. This defect could lead to system shutdowns.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Wilson-Cook Medical Recalls Nasal Jejunal Feeding Tube Over Missing Component
Wilson-Cook Medical recalled 60 units of Nasal Jejunal Feeding Tube NJFT-10 on December 15, 2025. The tubes were packaged without the necessary nasal transfer tube component. This defect poses a high hazard risk for patients requiring feeding assistance.
Wilson-Cook Medical
Nasal feeding
Health & Personal Care
HIGH
FDA DEVICE
Immunotech A.S. Recalls Estrone RIA Kit Over False Results Hazard
Immunotech A.S. recalled 160 Estrone RIA kits on December 15, 2025, due to a risk of falsely high patient results. This class II recall affects kits distributed in multiple countries, including the US and several European nations.
Immunotech A.S.
The affected
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Recalls Allura Xper FD10 Over Electrical Hazard
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips has
Health & Personal Care
HIGH
FDA DEVICE
ICU Medical Recalls Plum Duo Infusion System Over Speaker Failure
ICU Medical recalled 423 units of the Plum Duo Infusion System on December 15, 2025. Defective primary speakers may fail to produce audible alarms and alerts. This poses a high hazard risk to patients reliant on the device for medication administration.
ICU Medical
ICU Medical
Health & Personal Care
HIGH
FDA DEVICE
Sysmex America Recalls Tube Sorter Due to Lift Hazard
Sysmex America recalled 44 units of the TS-10/TS-10H Tube Sorter on December 15, 2025. The electromagnetic holding force may disengage, causing unintended movement. Healthcare providers should stop using the device immediately.
Sysmex America
Under specific
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Recalling Allura Xper FD10 Over Electrical Risk
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Broselow Recall: Harmful Dosing Errors in Pediatric Organizer
Broselow recalled 89 units of the BROSELOW FILLED BROSELOW ORGANIZER on December 15, 2025. The product contains harmful dosing errors for critical medications. Healthcare providers must stop using the device immediately.
SunMed Holdings
Product contains
Health & Personal Care
HIGH
FDA DEVICE
Philips Recalls Allura Xper FD20 Biplane Over Electrical Hazard
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Hologic Recalls Brevera Breast Biopsy System Due to Contamination Hazard
Presence of particulates in affected devices that can be deposited into breast tissue during use.
Hologic
Presence of
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