FDA Medical Device Recalls (openFDA)
Terumo Medical Corporation: Terumo Sur-vet Needle, 22G x 3/4", Product Code 100279
- Recall number
- Z-2002-2019
- Recalling firm
- Terumo Medical Corporation
- Product
- Terumo Sur-vet Needle, 22G x 3/4", Product Code 100279
- Status
- Terminated
- Initiated
- 2019-02-08
- Posted
- not on file
- Terminated
- 2020-05-08
- Reason
- There is a potential for a loss of package integrity that may compromise the sterility of the product.
- Root cause
- Packaging
- Action
- Urgent Voluntary Medical Device Recall notification letters dated 2/8/19 were sent to customers.
- Quantity
- 844,000
- Distribution
- The products were distributed to the following US states: FL, IN, KS, KY, MA, MO, NH, NV, PA, SC, TN, and TX.
- Lot, serial or model codes
- Lot Numbers 180705C 180814C 180829C
- 510(k) numbers
- ["K121607"]
- PMA numbers
- not on file
- Product code
- FMI
- Firm FEI
- 1118880
- Firm city
- Elkton
- Firm state
- MD
- 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