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.
Showing 30821–30840 of 38,428 recalls
Recalled Item: VACUUM TUBING 7/8" X 6' (2.22cm X 182.88cm)
The Issue: This recall is being conducted because a cohesive
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRAL WAND W/TUBING
The Issue: This recall is being conducted because a cohesive
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (S) TUBE SET 1/4" X 10' (0.64 cm X 304.8 cm) with 7/8" (2.22 cm) Adaptor
The Issue: This recall is being conducted because a cohesive
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FREEDOMAIRE(R) HELMET SYSTEM WITH SUPER POWER PAK BATTERY
The Issue: This recall is being conducted because a cohesive
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FREEDOMAIRE(R) HELMET SYSTEM WITH BELT
The Issue: This recall is being conducted because a cohesive
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FREEDOMAIRE(R) HELMET WITH MOTOR MODULE
The Issue: This recall is being conducted because a cohesive
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smoke Evacuation Tubing Set for Coherent CPG Handpiece
The Issue: This recall is being conducted because a cohesive
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FREEDOMAIRE(R) MOTOR MODULE
The Issue: This recall is being conducted because a cohesive
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUBING SET 7/8" X 6' WITH 1/4" x 24" TUBING
The Issue: This recall is being conducted because a cohesive
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUBING 7/8' X 10'
The Issue: This recall is being conducted because a cohesive
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LAPAROSCOPIC TUBING SET
The Issue: This recall is being conducted because a cohesive
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona¿ Anterior Sizer with Locking Boom The
The Issue: Zimmer, Inc is voluntarily recalling 22 lots of
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUUM TUBING 7/8" X 6' (2.22cm X 182.88cm)
The Issue: This recall is being conducted because a cohesive
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASER RESISTANT WAND - STERILE
The Issue: This recall is being conducted because a cohesive
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujifilm Endoscope Models ED-250XL5 ED-250XT5 ED-450XT5 ED-450XL5 Product...
The Issue: Fujifilm is conducting a corrective action due to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujifilm Endoscope Model ED-530XT Product Usage: This product is a
The Issue: Fujifilm is reporting a corrective action due to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TS ROC Crown Component 4UR (5/pk)
The Issue: The Universal Nut, a component of the orthodontic
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Specialty MiniScope Mech. Set Size 18
The Issue: The Universal Nut, a component of the orthodontic
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TS Herbst Nuts with Backing (10/pk) and TS Herbst Nuts
The Issue: The Universal Nut, a component of the orthodontic
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniScope Hst ROC Crown 15 Patient Kit
The Issue: The Universal Nut, a component of the orthodontic
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.