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 II14CM ANGLE ATTACHMENT, BLACK MAX
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class II10.5CM ANGLE ATTACHMENT, BLACK MAX
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class II11CM ANGLE ATTACHMENT, BLACK MAX
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class II90 DEG RIGHT ANGLE ATTACH, BLACK MAX
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IICONTRA ANGLE ATTACHMENT, BLACK MAX
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class II9.4CM MICRO REVISION ATTACH, BLACK MAX
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class II16.5CM MICRO REVISION ATTACH, BLACK MAX
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class II22CM MICRO REVISION ATTACH, BLACK MAX
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IIKEYLESS DRIVER, BLACK MAX
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class II16CM MIN INVASIVE ATTACH, BLACK MAX
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IIADJUSTABLE DRILL GUIDE, BLACK MAX
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IIGREEN ROTATING CRANIOTOME, BLACK MAX
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IISTANDARD CRANIOTOME, BLACK MAX
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IILARGE CRANIOTOME, BLACK MAX
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class II11.25CM ATTACHMENT, BLACK MAX
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class II19CM ATTACHMENT, BLACK MAX
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class II7.2cm Adjustable Drill Guide Product Usage: Electric system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IISystem Console, Single Port, no irrigation
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IISystem Console, Single Port, with irrigation Product Usage: Electric system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IIConsole, eMax2 Plus Product Usage: Electric system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IIFoot Control without Switches, SC2100 Product Usage: Electric system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IIFoot Control, SC2100 Product Usage: Electric system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IIeMax2 PLUS Product Usage: Electric system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IIeMax2 Hybrid Hand Control Product Usage: Electric system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IIeMax2 Motor Assembly Product Usage: Electric system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IIElectronic Foot Control with Direction or Irrigation Switches Product Usage: Electric system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IIElectronic Foot Control with Direction Switch Product Usage: Electric system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IIElectric Handpiece EM Hand Control Product Usage: Electric system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IIElectronic Foot Control with Direction or Irrigation Switches Product Usage: Electric system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
- 2017-05-10FDA-DeviceThe Anspach Effort, Inc.Class IIXMAX Motor, High Strength Hose Product Usage: Pneumatic system
Supplied Directions for Use (DFU) did not contain a recommended service interval.
Get notified about new device recalls
Free weekly digest. We email when a new federal recall in this category — or anything else affecting your household — is published.
Get the Sunday Brief