HIGHFDA DEVICE

Medline Recalls Arthroscopy Kits Over Sterility Concerns

Medline Industries recalled 175 arthroscopy kits on January 7, 2026. Calibration issues with sterilization equipment may impact product sterility. Patients and healthcare providers should stop using the devices immediately.

Official notice
Medline Industries, LPHealth & Personal CareMedical Devices1) CDS984609BUDI-DI: 10889942719372(each)40889942719373(case)

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
January 7, 2026
Status
ACTIVE
Severity
8/10

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

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 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.

  1. Recall announced

    January 7, 2026

  2. Reported by FDA DEVICE

    February 25, 2026

  3. RecallRadar source check

    March 4, 2026

  4. 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

  1. Check the model numbers on the packaging or product itself.
  2. Look for lot numbers on the packaging: 23BBL738, 23BBJ847, 22IBF936, 22IBE795, 22FBP788 to identify affected kits.
  3. 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.

Get instant alerts for Health & Personal Care recalls

Be the first to know. Free instant alerts to your inbox.

No spamUnsubscribe anytime

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

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

Get Alerts for Health & Personal Care Recalls

Get instant alerts for recalls that affect you. Free forever.

Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Details

Model Numbers
1) CDS984609B
UDI-DI: 10889942719372(each)
40889942719373(case)
Lot Number: 23BBL738
2) CDS984609B
+7 more
Affected States
ALL
Report Date
February 25, 2026
Recall Status
ACTIVE

Related Recalls