Quick Facts at a Glance
- Recall Date
- January 7, 2026
- Hazard Level
- HIGH
- Brand
- Medline Industries, LP
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers
- 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
- Medline Industries, LP
- Product type
- Arthroscopy Kits
- Model numbers
- 1) CDS984609B, UDI-DI: 10889942719372(each), 40889942719373(case), Lot Number: 23BBL738, 2) CDS984609B, Lot Number: 23BBJ847, 3) CDS984609B, Lot Number: 22IBF936 +4 more
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
January 7, 2026
Reported by FDA DEVICE
February 25, 2026
RecallRadar source check
March 4, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
What You Should Do
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Medline Industries, LP or your healthcare provider for instructions. Notification method: Letter
About This Product
Medline's arthroscopy kits are used in surgical procedures to assist with minimally invasive joint surgeries. They provide essential tools and materials necessary for arthroscopic surgeries.
Why This Is Dangerous
The calibration issues with sterilization equipment may lead to insufficient sterilization of the products, increasing the risk of infection during surgical procedures.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
This recall affects healthcare providers and patients who may have used these kits, raising safety concerns about potential infections during surgeries.
Practical Guidance
How to identify if yours is affected
- Check the model numbers on the packaging or product itself.
- Look for lot numbers on the packaging: 23BBL738, 23BBJ847, 22IBF936, 22IBE795, 22FBP788 to identify affected kits.
- Verify the product against the recall list provided by Medline.
Where to find product info
Model numbers and lot numbers can typically be found on the product packaging or the device itself.
What timeline to expect
Expect a response for refund or replacement processing within 4-6 weeks.
If the manufacturer is unresponsive
- Document all correspondence with Medline regarding the recall.
- Consider contacting consumer protection agencies if no response is received after 4 weeks.
How to prevent similar issues
- Always check for recalls on medical devices before use.
- Ensure devices are certified by recognized safety standards before purchase.
Documentation advice
Keep records of your purchase, including receipts, correspondence regarding the recall, and photos of the product.
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Product Details
The recall involves Medline's arthroscopy kits, including models CDS984609B, DYNJ22501G, DYNJ32715F, DYNJ50834C, and DYNJ51069. The products were distributed worldwide and sold in the U.S. since their release.
Key Facts
- Calibration issues may affect sterility
- Stop using the products immediately
- Contact Medline for instructions
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Safety Guide
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