Skip to the content

FDA Medical Device Recalls (openFDA)

Zimmer Inc.: Trabecular Metal acetabular revision system column buttress right posterior/left anterior, 00-4894-400-00, sterile, Zimmer Inc., Parsippany, NJ.

Recall number
Z-2217-2010
Recalling firm
Zimmer Inc.
Product
Trabecular Metal acetabular revision system column buttress right posterior/left anterior, 00-4894-400-00, sterile, Zimmer Inc., Parsippany, NJ.
Status
Terminated
Initiated
2010-04-06
Posted
2010-08-12
Terminated
2011-10-21
Reason
The firm has determined that some of the packages could develop a breach of the seal in the sterile barrier pouches.
Root cause
Packaging
Action
The firm sent an "Urgent Device Removal" letter dated 4/6/2010. The consignees were instructed to inventory the products on hand and return the recalled product to the manufacturer. More information is available at 1-800-613-6131.
Quantity
1,972 all products
Distribution
US, Germany, Brazil, Singapore, Canada, Australia, England, India, and Switzerland.
Lot, serial or model codes
60492197, 60704071, 60667465, 60728122, 60770944, 60796679, 60862513, 61081548, 61143008, and 61324533.
510(k) numbers
["K061067"]
PMA numbers
not on file
Product code
LPH
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

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

Search this register