company
AVID Medical, Inc.
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_recall2026-06-17AVID Medical, Inc. — Class II recall: Halyard, Pain Pack. Kit Code: AMPK48-01.
- fda_recall · device_recall2026-06-17AVID Medical, Inc. — Class II recall: Halyard, Drape Pack. Kit Code: LMDP36-01.
- fda_recall · device_recall2026-06-17AVID Medical, Inc. — Class II recall: Halyard, Eye Bag Pack. Kit Code: UIEB48-01.
- fda_recall · device_recall2026-06-17AVID Medical, Inc. — Class II recall: Halyard, Towel Six Pack. Kit Code: AMTS70-01.
- fda_recall · device_recall2026-05-13AVID Medical, Inc. — Class I recall: Halyard PERC TRAY kit. Model Numbers: SLPC34-01, SLPC34-02.
- fda_recall · device_recall2026-05-13AVID Medical, Inc. — Class I recall: Halyard NEURO IR PERIPHERAL (PS 64405) kit. Model Number: UINR44-01.
- fda_recall · device_recall2026-05-13AVID Medical, Inc. — Class I recall: Halyard CARDIAC CATH PACK kit. Model Number: EAMC1000-05, WAFB208-02.
- fda_recall · device_recall2026-05-13AVID Medical, Inc. — Class I recall: Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04, SHND401-05.
- fda_recall · device_recall2026-05-13AVID Medical, Inc. — Class I recall: Halyard HEART CATH, SELF REGIONAL kit. Model Number: SELF131-05.
- fda_recall · device_recall2026-05-13AVID Medical, Inc. — Class I recall: Halyard SAMMC ANGIOGRAPHY kit. Model Numbers: SAMM066-15.
- fda_recall · device_recall2026-05-13AVID Medical, Inc. — Class I recall: Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC36.
- fda_recall · device_recall2026-05-13AVID Medical, Inc. — Class I recall: Halyard CATH LAB kit. Model Number: SACL75-01.
- fda_recall · device_recall2026-05-13AVID Medical, Inc. — Class I recall: Halyard VA DETROIT CATH LAB PACK kit. Model Numbers: VMCD029.
- fda_recall · device_recall2026-05-13AVID Medical, Inc. — Class I recall: Halyard CATH LAB kit. Model Number: SACL75AM.
Frequently asked questions
- How many FDA warning letters has AVID Medical, Inc. received?
- Argus HQ has not recorded an FDA warning letter for AVID Medical, Inc. in our current dataset.
- What FDA recalls has AVID Medical, Inc. issued?
- Argus HQ has recorded 14 FDA recalls tied to AVID Medical, Inc..
- Is AVID Medical, Inc. FDA compliant?
- Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 14 recalls, and 0 approval records for AVID Medical, Inc.. 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.