company
DJO, LLC
Jurisdiction: US
FDA Warning Letter timeline
V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.
- fda_recall · device_recall2026-05-20DJO, LLC — Class II recall: Brand Name: DONJOY Product Name: ICEMAN, W/COLDPAD, NS, RH Model/Catalog Numbe…
- fda_recall · device_recall2026-05-20DJO, LLC — Class II recall: Brand Name: DONJOY Product Name: ICEMAN W/,UNIV,LOOP,NS,RH Model/Catalog Numbe…
- fda_recall · device_recall2026-05-20DJO, LLC — Class II recall: Brand Name: DONJOY Product Name: ICEMAN CLASSIC CUBE Model/Catalog Number: 11-…
- fda_recall · device_recall2026-05-20DJO, LLC — Class II recall: Brand Name: DONJOY Product Name: ICEMAN W/,UNIV,LOOP,NS,EH Model/Catalog Numbe…
Frequently asked questions
- How many FDA warning letters has DJO, LLC received?
- Argus HQ has not recorded an FDA warning letter for DJO, LLC in our current dataset.
- What FDA recalls has DJO, LLC issued?
- Argus HQ has recorded 4 FDA recalls tied to DJO, LLC.
- Is DJO, LLC FDA compliant?
- Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 4 recalls, and 0 approval records for DJO, LLC. Review the linked FDA source records directly before drawing a compliance conclusion.
Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.