FDA Medical Device Recalls (openFDA)
DeRoyal Industries Inc: Custom medical procedure packs labeled as: a) STURDI STRAINER TRAY STANDARD, REF '89-5014
- Recall number
- Z-2087-2023
- Recalling firm
- DeRoyal Industries Inc
- Product
- Custom medical procedure packs labeled as: a) STURDI STRAINER TRAY STANDARD, REF '89-5014
- Status
- Open, Classified
- Initiated
- 2023-05-30
- Posted
- 2023-07-03
- Terminated
- not on file
- Reason
- The outer package seal could be open, or compromised which affects the sterility of the procedure pack inside.
- Root cause
- Process control
- Action
- DeRoyal disseminated an URGENT! DEROYAL RECALL NOTICE to its consignees on 05/30/2023 by email. The notice explained the issue, the risk, and requested the return of the affected products. Distributors were also directed to identify and notify their customers.
- Quantity
- 40 units
- Distribution
- US Nationwide distribution.
- Lot, serial or model codes
- a) REF '89-5014, GTIN 50749756217908 (cs), 00749756217903 (unit) Lot Numbers: 58770294
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FNY
- Firm FEI
- 1043214
- Firm city
- Powell
- Firm state
- TN
- 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