Quick Facts at a Glance
- Recall Date
- February 5, 2026
- Hazard Level
- HIGH
- Brand
- Remel
- Category
- Health & Personal Care
- Sold At
- Unknown
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Remel
- Product type
- Medium for Campylobacter Jejuni Testing
- Model numbers
- UDI-DI 848838001055 Lot R01272 lot 339135 Expired January 12, 2026
- Sold at
- Unknown
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
February 5, 2026
Reported by FDA DEVICE
March 4, 2026
RecallRadar source check
March 11, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.
What You Should Do
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Remel, Inc or your healthcare provider for instructions. Notification method: Letter
About This Product
Campy CVA Medium is used in laboratories for the testing of Campylobacter Jejuni, a bacteria causing gastrointestinal illness. Laboratories purchase this medium to ensure accurate testing results.
Why This Is Dangerous
The identified lot of medium has shown low to no recovery of the bacteria, which compromises the reliability of test results and can lead to misdiagnosis.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Patients and healthcare providers relying on this medium may face delays in accurate testing, potentially impacting patient care.
Practical Guidance
How to identify if yours is affected
- Locate the product packaging and check for the lot number R01272.
- Verify the expiration date, which is January 12, 2026.
- Consult with your healthcare provider about the recall.
Where to find product info
The lot number and expiration date can typically be found on the product label or packaging.
What timeline to expect
Expect a timeline of 4-8 weeks for any refunds or replacements associated with the recall.
If the manufacturer is unresponsive
- Document all communication attempts with Remel, Inc.
- Reach out to the FDA if the company does not respond.
- Keep a record of your correspondence for future reference.
How to prevent similar issues
- Check for FDA recalls before purchasing laboratory products.
- Look for quality assurances or certifications from manufacturers.
- Always verify expiration dates on laboratory media.
Documentation advice
Keep copies of any receipts, correspondence, and photographs of the product for your records.
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Product Details
The recalled product is Campy CVA Medium, with model UDI-DI 848838001055 and lot number R01272. It has an expiration date of January 12, 2026. The product was distributed nationwide in states including AZ, CO, IL, NJ, OH, TN, and WA.
Key Facts
- Low recovery of Campylobacter Jejuni ATCC 33291
- Nationwide distribution across several states
- Expiration date: January 12, 2026
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Safety Guide
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