Medical device recalls
39229 federal recalls on file. Federal recalls for medical devices — surgical equipment, monitors, diagnostic tools, implants, home health devices. Sourced from the FDA.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IIBearing Sleeve, 10CM Straight Product Usage: Pneumatic system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IIBearing Sleeve, 10CM Curved Product Usage: Pneumatic system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class II10.5cm Long Attachment Product Usage: Pneumatic system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class II12.4cm Heavy Duty Long Heavy Short Attachment Product Usage: Pneumatic system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class II10.5cm Long Attachment, Non-Tapered End Product Usage: Pneumatic system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class II11.0cm Long Attachment Product Usage: Pneumatic system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IIIMRI SHORT HD ATTACHMENT Product Usage: Pneumatic system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IIIMRI SHORT ATTACHMENT Product Usage: Pneumatic system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IIIMRI CRANI-A ATTACHMENT Product Usage: Pneumatic system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IIKeyless Driver Product Usage: Pneumatic system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IIChuck Driver System
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IICompact Speed Reducer, 60:1 Black Max
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IICompact Speed Reducer, 60:1
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IIPediatric Craniotome
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IIRotating Large Craniotome
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IILarge Craniotome Product Usage: Pneumatic system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IIRotating Adult Craniotome Product Usage: Pneumatic system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class II6.5CM ADLT CRANI, THIN FT PLATE Product Usage: Pneumatic system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IIAdult Craniotome Product Usage: Pneumatic system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class II6.8cm Controlled Depth Attachment Product Usage: Pneumatic system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class II8.2CM ATTACHMENT, BLACK MAX Product Usage: Pneumatic system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IIPEDIATRIC CRANIOTOME, BM Product Usage: Pneumatic system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class II5.9CM ATTACHMENT, BLACK MAX Product Usage: Pneumatic system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class II12.6CM TAPERED ATTACHMENT, BLACK MAX Product Usage: Pneumatic system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class II6.1CM ATTACHMENT, BLACK MAX Product Usage: Pneumatic system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IIB-SAGITTAL ASSEMBLY Product Usage: Pneumatic system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class II26.65CM ATTACHMENT, BLACK MAX
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class II7.5CM ANGLE ATTACHMENT, BLACK MAX
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class II8CM ANGLE ATTACHMENT, BLACK MAX
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class II13.5CM ANGLE ATTACHMENT, BLACK MAX
Supplied Directions for Use (DFU) did not contain a recommended service interval.
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