Surgical Device Recalls
1-10 of 35
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Zimmer Biomet Recalls More than 3,600 Shoulder Implants Due to a High Fracture Rate
Posted 02/21/17 | 
Teleflex Recalls Anesthesia Circuits
Devices may crack, hindering airway-based care.
Posted 10/08/14 |
Johnson & Johnson Asks Customers to Return Morcellators
Impassioned debate accompanies decision.
Posted 08/04/14 |
Hospira Recalling Propofol, Lidocaine
Posted 04/21/14 |
Recalled Tracheal Tube Could be Deadly
Teleflex says product can kink during use.
Posted 02/14/14 |
Electrical Issue Sparks Anesthesia Machine Recall
4 Draeger Medical products affected, FDA reports.
Posted 10/23/13 |
Hospira Recalls 2 Lots of Bupivacaine
Both may contain dangerous particulates.
Posted 09/16/13 |
FDA Says Recalled Stryker Device is Potentially Deadly
Spinal implant recall is now Class 1.
Posted 08/30/13 |
Depuy Orthopaedics Recalls Lower Leg Implant
The FDA warns surgeons to immediately stop using the device.
Posted 08/05/13 |
Verathon Recalls Its Video Laryngoscope Reusable Blades
Fears of breakage and premature failure prompted the action.
Posted 07/11/13 |
