ClearanceBrief
Recall Z-2257-2025 ยท OKV Obstetrical Kit

AVID Medical, Inc.

LAVH PACK. Medical convenience kit.

DateAug 4, 2025 (initiated Jun 11, 2025)
StatusOpen, Classified
ReasonCLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
Root causeUnder Investigation by firm
ActionConsignees were sent an URGENT: MEDICAL DEVICE FIELD CORRECTION notice, dated 6/11/25, via email. The notification instructs consignees to not use the CLEARIFY Visualization System (component #5303907) and discard. All other components in the kit may be continued to be used. Consignees are to add warning labels to affected procedure trays to ensure the affected component is discarded. The provided Recall Response Form is to be completed and returned to Owens&Minor. Any quality problems or adverse events associated with recalled devices may be reported via email to complaints@owens-minor.com
Quantity292 units
DistributionDomestic: CA, IL, MD, OH, PA, TX, WA.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.