FDA Medical Device Recalls (openFDA)
Inmar Supply Chain Solutions, LLC: Various Medical Products stored on pallets, including but not limited to bandages, tampons, condoms, blood glucose monitors, adult diapers, COVID-19 test kits, and pregnancy tests.
- Recall number
- Z-2634-2023
- Recalling firm
- Inmar Supply Chain Solutions, LLC
- Product
- Various Medical Products stored on pallets, including but not limited to bandages, tampons, condoms, blood glucose monitors, adult diapers, COVID-19 test kits, and pregnancy tests.
- Status
- Open, Classified
- Initiated
- 2023-08-24
- Posted
- 2023-09-25
- Terminated
- not on file
- Reason
- Various medical devices potentially exposed to rodent and rodent activity. In addition, medical devices may have been subjected to temperatures in excess of storage requirements on product labeling.
- Root cause
- Unknown/Undetermined by firm
- Action
- Beginning on August 15, 2023, Inmar Supply Chain Solutions, LLC notified consignees via email and company website concerning a voluntary recall. On August 23, 2023, Inmar issued a press release concerning the matter. The recall instructions are for the products to be destroyed by the liquidation buyer.
- Quantity
- unknown
- Distribution
- US Nationwide distribution.
- Lot, serial or model codes
- Various
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- N/A
- Firm FEI
- 3009127711
- Firm city
- Arlington
- 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