FDA Medical Device Recalls (openFDA)
Zimmer GmbH: Drill, cannulated, 4x90mm, round shaft, Item Number 502015640
- Recall number
- Z-1450-2019
- Recalling firm
- Zimmer GmbH
- Product
- Drill, cannulated, 4x90mm, round shaft, Item Number 502015640
- Status
- Terminated
- Initiated
- 2019-04-08
- Posted
- not on file
- Terminated
- 2020-05-11
- Reason
- An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
- Root cause
- Under Investigation by firm
- Action
- Urgent Medical Device Recall notification letters dated 4/8/19 were sent to customers.
- Quantity
- not on file
- Distribution
- The products were distributed to the following US states: AL, AR, AZ, CA, CO, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV, and WY.
- Lot, serial or model codes
- All items marked with "Normed" are affected
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- HTW
- Firm FEI
- 3005233524
- Firm city
- Winterthur
- Firm state
- not on file
- Firm country
- Switzerland
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28