- Recalling firm
- DJO, LLC
- Reason for recall
- Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
- Affected products (lot / model / serial)
- Model/Catalog Number: 11-9099 Lot Code: Lot: 110525 GTIN: 00888912000376
- Units affected
- 96
- Distribution pattern
- Worldwide - U.S. Nationwide distribution in the states of AK, AL, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KY, LA, MA, MD, MI, MO, NC, NE. NY, OH, OK, PA, SC, SD, TN, TX, UT, VA, WA, WI, and WV. The country of Canada.
- Firm location
- Carlsbad, CA, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2137-2026
- Recall initiated
- March 19, 2026
- FDA classification date
- May 8, 2026
- FDA report date
- May 20, 2026
- FDA event ID
- 98638
- Last updated on HTM Vibe
- July 24, 2026