FDA Medical Device Recalls (openFDA)
Remel Inc: Thermo Scientific Sensititre Gram Negative Susceptibility Testing Plate, IVD format
- Recall number
- Z-0722-2022
- Recalling firm
- Remel Inc
- Product
- Thermo Scientific Sensititre Gram Negative Susceptibility Testing Plate, IVD format
- Status
- Open, Classified
- Initiated
- 2022-01-10
- Posted
- not on file
- Terminated
- not on file
- Reason
- There are lower than expected MICs for some gram negative species.
- Root cause
- Under Investigation by firm
- Action
- A customer letter was issued to impacted consignees on or around 01/10/2022. Customers are asked to check for affected product and the recalling firm requests that customers do not report results of cefiderocol when affected product is used with Thermo Scientific Mueller-Hinton Broth with TES, catalong T3462, lots 267261 to 402775. Consignees are asked to disseminate the recall information within their organization and to any other organization to which affected products have been transferred. An acknowledgement form should be submitted by email to MBD.vigilance@thermofisher.com.
- Quantity
- 1210 devices
- Distribution
- Distribution throughout the United States.
- Lot, serial or model codes
- Product Number MDRGN2F; Lots: 1) B1402A (Expiration 2022/Oct05) 2) B1315A (Expiration 2022/Aug06) 3) B1211 (Expiration 2022/May24) 4) B1161A (Expiration 2022/Apr19 5) B0361 (Expiration 2021/Aug31) 6) B0164B (Expiration 2021/Apr16)
- 510(k) numbers
- ["K193538"]
- PMA numbers
- not on file
- Product code
- JWY
- Firm FEI
- 1924669
- Firm city
- Lenexa
- Firm state
- KS
- 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