Browse Device Recalls

261 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 261 FDA medical device recall enforcement actions. Each entry includes the device description, reason for recall, classification (Class I through III based on severity), recalling firm, and distribution details. Use the filters below to search by year, classification, state, or keyword.

Medical Device Recalls

Browse 261 FDA device recalls.

Clear
DateProductReasonClassFirm
Dec 7, 2022 Adult Craniotome Ref: CRANI-A-G1 Intended for cutting and shaping bone i... Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the at... Class II The Anspach Effort, Inc.
Dec 7, 2022 6.5 cm Adult Rotating Craniotome Attachment. Use with XMax¿, microMax, and eM... Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the at... Class II The Anspach Effort, Inc.
Dec 7, 2022 6.5 cm Adult Craniotome, Thin Foot Plate Attachment. Use with XMax¿, microMa... Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the at... Class II The Anspach Effort, Inc.
Dec 7, 2022 6.5 cm Adult Rotating Craniotome Attachment. Use with XMax¿, microMax, and eM... Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the at... Class II The Anspach Effort, Inc.
Dec 7, 2022 7.5 cm Large Craniotome Attachment Use with XMax¿, microMax, and eMax¿ Syste... Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the at... Class II The Anspach Effort, Inc.
Dec 7, 2022 6.5 cm Pediatric Craniotome Attachment. Use with XMax¿, microMax, and eMax¿ S... Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the at... Class II The Anspach Effort, Inc.
Dec 7, 2022 7.5 cm Large Rotating Craniotome Attachment. Use with XMax¿, microMax, and eM... Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the at... Class II The Anspach Effort, Inc.
Dec 7, 2022 Adult Craniotome, Large Ref: CRANI-L-G1 Intended for cutting and shaping... Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the at... Class II The Anspach Effort, Inc.
Dec 7, 2022 Pediatric Craniotome Ref:CRANI-P-G1 Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the at... Class II The Anspach Effort, Inc.
Sep 29, 2017 OSCILLATING SAW ATTACHMENT Surgical instrument motors and accessories/atta... This voluntary recall was initiated because a veterinary unit was physically shipped in error to ... Class II The Anspach Effort, Inc.
Oct 6, 2016 Autolube-III Product Usage: Pneumatic system Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 PEDIATRIC CRANIOTOME, BM Product Usage: Pneumatic system Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 Bearing Sleeve, 10CM Curved Product Usage: Pneumatic system Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 AL-III W/ male disconnect and 20ft hose Product Usage: Pneumatic system Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 5.9CM ATTACHMENT, BLACK MAX Product Usage: Pneumatic system Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 IMRI SHORT HD ATTACHMENT Product Usage: Pneumatic system Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 8.0cm Medium Attachment Product Usage: Pneumatic system Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 Otologic Curved Micro Product Usage: Pneumatic system Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 6.5CM ADLT CRANI, THIN FT PLATE Product Usage: Pneumatic system Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 Bearing Sleeve, 15CM Straight Taper Product Usage: Pneumatic system Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 16cm Minimally Invasive Attachment Product Usage: Pneumatic system Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 Minimal Access Attachment Product Usage: Pneumatic system Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 Minimal Access Attachment, BLACK MAX Product Usage: Pneumatic system Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 Sagittal Saw Product Usage: Pneumatic system Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 19CM ATTACHMENT, BLACK MAX Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 Console, eMax2 Plus Product Usage: Electric system Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 Chuck Driver System Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 SMALL ATTACHMENT, JACOBS CHUCK Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 Minimal Access Straight Driver Product Usage: Pneumatic system Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 B-SAGITTAL ASSEMBLY Product Usage: Pneumatic system Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 7.2cm Adjustable Drill Guide Product Usage: Electric system Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 8CM ANGLE ATTACHMENT, BLACK MAX Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 11.25CM ATTACHMENT, BLACK MAX Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 10.5CM ANGLE ATTACHMENT, BLACK MAX Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 KEYLESS DRIVER, BLACK MAX Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 LARGE CRANIOTOME, BLACK MAX Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 16.5CM MICRO REVISION ATTACH, BLACK MAX Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 8.2CM ATTACHMENT, BLACK MAX Product Usage: Pneumatic system Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 Oscillating MICRO-SAW Product Usage: Pneumatic system Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 14cm QD Angle Attachment Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 Pediatric Craniotome Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 XMAX Motor (Pneumatic Drill System) Product Usage: Pneumatic system Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 Sagittal MICRO-SAW Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 5.0cm Heavy Duty Short Attachment Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 20.2cm Heavy Duty Long Heavy Short Attachment Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 Adult Craniotome Product Usage: Pneumatic system Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 AL-III W/ male disconnect and 30ft hose Product Usage: Pneumatic system Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 Electronic Foot Control with Direction or Irrigation Switches Product Usag... Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 Autolube-III with NK Product Usage: Pneumatic system Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.
Oct 6, 2016 22CM MICRO REVISION ATTACH, BLACK MAX Supplied Directions for Use (DFU) did not contain a recommended service interval. Class II The Anspach Effort, Inc.

Frequently Asked Questions

When a device safety issue is identified, the manufacturer or FDA initiates a recall. The FDA publishes an enforcement report detailing the device, the reason for the recall, and distribution. Healthcare facilities and providers are notified to check their inventory and take corrective action.

All types — from simple devices like blood glucose test strips and surgical gloves to complex devices like pacemakers, defibrillators, insulin pumps, hip implants, and ventilators. Software-driven devices are increasingly common in recalls due to bugs and cybersecurity vulnerabilities.

Use the search and filter tools on this page. Each recall entry includes the device description, model numbers, and distribution details so you can determine if your device is affected. Contact your healthcare provider if you find a match.