Medical Device Recalls

This is our largest category by volume. The FDA tracks recalls for an enormous range of medical devices: implants, pacemakers, insulin pumps, surgical tools, blood glucose monitors, X-ray machines, prosthetics, contact lenses, and home health equipment, among many others. We have records dating back to 2005 and add new ones as the FDA publishes them.

Device recalls can happen because of software bugs, manufacturing defects, bacterial contamination, incorrect labeling, or design flaws that lead to inaccurate results or equipment failure. Class I recalls are the most serious and mean the device could cause injury or death.

38,428 total recalls
0 this month

Showing 6061–6080 of 38,428 recalls

January 31, 2024· Randox Laboratories Ltd.

Recalled Item: Microalbumin Calibrator Series (mALB CAL)-IVD used to calibrate the Microalbumin

The Issue: Microalbumin Calibrator Series, MA1567 & MA2426, is running

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
January 31, 2024· Randox Laboratories Ltd.

Recalled Item: Microalbumin Calibrator Series (mALB CAL)-IVD to calibrate the Microalbumin...

The Issue: Microalbumin Calibrator Series, MA1567 & MA2426, is running

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
January 31, 2024· Technicality Inc.

Recalled Item: Trumpet

The Issue: The Ring on the Trump Needle Guide can

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
January 30, 2024· Applied Medical Resources Corp

Recalled Item: Epix Universal Clip Applier

The Issue: Their is the potential that Universal Clip applier

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
January 30, 2024· Applied Medical Resources Corp

Recalled Item: Epix Universal Clip Applier

The Issue: Their is the potential that Universal Clip applier

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
January 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 NI/TU

The Issue: Non-conformance may prevent the guidewire from passing through

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
January 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 SS/SS

The Issue: Non-conformance may prevent the guidewire from passing through

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
January 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 4F X 10 CM STD .018 NI/TU

The Issue: Non-conformance may prevent the guidewire from passing through

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
January 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 NI/TU

The Issue: Non-conformance may prevent the guidewire from passing through

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
January 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 4F X 10 CM STD .018 SS/PD

The Issue: Non-conformance may prevent the guidewire from passing through

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
January 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 4F X 10 CM STIFF .018 SS/PD

The Issue: Non-conformance may prevent the guidewire from passing through

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
January 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STIFF .018 NI/TU

The Issue: Non-conformance may prevent the guidewire from passing through

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
January 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 SS/SS

The Issue: Non-conformance may prevent the guidewire from passing through

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
January 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 4F X 10 CM STIFF .018 SS/SS

The Issue: Non-conformance may prevent the guidewire from passing through

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
January 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 4F X 10CM STIFF .018 NI/TU ECHO

The Issue: Non-conformance may prevent the guidewire from passing through

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
January 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 SS/SS

The Issue: Non-conformance may prevent the guidewire from passing through

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
January 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STIFF .018 SS/PD

The Issue: Non-conformance may prevent the guidewire from passing through

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
January 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 4F X 10 CM STIFF .018 NI/TU

The Issue: Non-conformance may prevent the guidewire from passing through

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
January 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 15 CM STIFF .018 NI/TU

The Issue: Non-conformance may prevent the guidewire from passing through

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
January 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 SS/SS

The Issue: Non-conformance may prevent the guidewire from passing through

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing