Z-1474-2026Class II

Campy CVA Medium 100/PK, R01272

Name: Z-1474-2026 Campy CVA Medium 100/PK, R01272
Creator: Remel, Inc
Published: 2026-02-05
License: https://open.fda.gov/license/

Remel Inc / initiated 2026-02-05 / Open, Classified

FDA source

Remel, Inc began a recall of Campy CVA Medium 100/PK, R01272 on 2026-02-05. FDA classified it as Class II and gives the reason as "Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium". As of 2026-09-10, the recall status on record is Open, Classified.

Recall record

Recall number: Z-1474-2026
Classification: Class II
Status: Open, Classified
Initiated: 2026-02-05
Posted: 2026-02-26
Recalling firm: Remel Inc
Product: Campy CVA Medium 100/PK, R01272
Product code: JSJ Culture Media, Selective And Non-Differential
Reason for recall: Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.
FDA root cause: Under Investigation by firm
Action: On February 5, 2026, the firm notified affected customers via Urgent Medical Device Recall letter. Customers were instructed to review test results and destroy any remaining inventory of the affected lot.
Quantity in commerce: 97
Distribution: US Nationwide distribution in the states of AZ, CO, IL, NJ, OH, TN, WA.
Product codes and lots: UDI-DI 848838001055 Lot R01272 lot 339135 Expired January 12, 2026

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-1474-2026
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-1474-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-03-04	2026-02-26

Product code JSJ

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)