FDA Medical Device Recalls (openFDA)
Zimmer Inc.: Zimmer Hemovac Wound Drainage Device Infection Control Kits, Catalog Number/ REF 00-2550-002-10, 400 ml-INF. Cntrl. Kit w/ 1/8" drain, 3.2 mm, 10Fr, PVC, 107 cm, medium, sterile, latex free, Rx only; Sold in packages of 10, which contain packages of 1 and 5; Zimmer U.K. Ltd., Swindon, Wiltshire, United Kingdom; Zimmer, Dover, Ohio
- Recall number
- Z-1449-2008
- Recalling firm
- Zimmer Inc.
- Product
- Zimmer Hemovac Wound Drainage Device Infection Control Kits, Catalog Number/ REF 00-2550-002-10, 400 ml-INF. Cntrl. Kit w/ 1/8" drain, 3.2 mm, 10Fr, PVC, 107 cm, medium, sterile, latex free, Rx only; Sold in packages of 10, which contain packages of 1 and 5; Zimmer U.K. Ltd., Swindon, Wiltshire, United Kingdom; Zimmer, Dover, Ohio
- Status
- Terminated
- Initiated
- 2008-01-31
- Posted
- 2008-04-09
- Terminated
- 2009-11-12
- Reason
- Leakage: The kits may disassemble at the fluid collection port, which would present a risk of exposure to blood borne pathogens to health care providers should it occur during use.
- Root cause
- Process control
- Action
- Consignees were notified via Urgent Infection Control Recall letter dated 1/31/08 to examine their inventory and return the recalled lots. Custom kit packers were instructed in the same letter to recall these products/lots from their own customers.
- Quantity
- 34,354 (Recalls Z-1448/1458-2008)
- Distribution
- Worldwide-USA, Australia, Canada, Colombia, Denmark, Dubai, Italy, Japan, Mexico and Singapore.
- Lot, serial or model codes
- Lot Numbers: 33440800, 60006818, 60015773, 60025362, 60033385, 60047775, 60051617, 60060757, 60067687, 60072831, 60082265, 60090133, 60096160, 60102772, 60108662, 60118934, 60129193, 60139016, 60147493, 60154829, 60163266, 60171588, 60181669, 60190630, 60196964, 60203044, 60212869, 60223951, 60233568, 60245183, 60252225, 60266735, 60278451, 60288208, 60305457, 60317372, 60323772, 60331175, 60339076, 60346591, 60359577, 60372899, 60382573, 60391905, 60401085, 60409371, 60419370, 60430869, 60444464, 60463237, 60475741, 60488170, 60496915, 60511108, 60530243, 60546074, 60565010, 60578962, 60594499, 60607928, 60622522, 60626621 and 60640519.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- GCY
- 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