FDA Medical Device Recalls (openFDA)
Life-Tech International, Inc: ProLong Continuous Nerve Block Set model nubers PL-50 and PL-100
- Recall number
- Z-1003-03
- Recalling firm
- Life-Tech International, Inc
- Product
- ProLong Continuous Nerve Block Set model nubers PL-50 and PL-100
- Status
- Terminated
- Initiated
- 2001-05-09
- Posted
- 2003-07-15
- Terminated
- 2003-07-15
- Reason
- Catheter does not fit through the needle resulting in delay of medical procedure
- Root cause
- Other
- Action
- The firm initiated the recall via letter to all consignees on May 9, 2001.
- Quantity
- not on file
- Distribution
- CA, MN, TX, FL, UT,
- Lot, serial or model codes
- All manufacturing codes were recalled. Model numbers: PL-50, PL-100
- 510(k) numbers
- ["K001129"]
- PMA numbers
- not on file
- Product code
- CAZ
- Firm FEI
- 1625424
- Firm city
- Stafford
- Firm state
- TX
- 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