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FDA Medical Device Recalls (openFDA)

Zimmer Inc.: Zimmer Minimally Invasive Solutions Technology Offset Rasp Handle, Right, 45 degrees, non-sterile; REF 7712-35-02, Zimmer U.K. Ltd., SN3, 4FP, UK

Recall number
Z-0317-2008
Recalling firm
Zimmer Inc.
Product
Zimmer Minimally Invasive Solutions Technology Offset Rasp Handle, Right, 45 degrees, non-sterile; REF 7712-35-02, Zimmer U.K. Ltd., SN3, 4FP, UK
Status
Terminated
Initiated
2007-06-28
Posted
2007-12-15
Terminated
2008-03-17
Reason
Clip Detachment: The retainer c-clip can detach from the instrument during use and may fall into the surgical wound
Root cause
Process control
Action
Zimmer notified their distributors via Product Recall Notification Letter dated 6/30/07 and instructed them to notify their customers of the recall and to pick up the product and return it to Zimmer.
Quantity
62 (total for Z-0316-0317-2008)
Distribution
Worldwide: USA including states of Arizona, California, Florida, Georgia, Indiana, Michigan, New York, North Carolina, and Virginia, and countries of Germany and Japan.
Lot, serial or model codes
Lot No: 60651168 and 60726506.
510(k) numbers
not on file
PMA numbers
not on file
Product code
LXH
Firm FEI
1000220733
Firm city
Warsaw
Firm state
IN
Firm country
not on file

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

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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

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