Manufacturer
207 recalls in our database name AVID Medical, Inc. as the manufacturing or recalling firm.
Of the 207 recalls from AVID Medical, Inc. we have scored against our rubric, 7 (3%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 21 (10%) are Severe.
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
Avid Medical is recalling 52 TruCustom PV Minor Pack convenience kits because they may contain needles with loose polypropylene foreign material.
Avid Medical is recalling 330 QA Packs because the included swab stick expires before the kit's expiration date.
Avid Medical is recalling 25,308 Vacutainer tubes because an expired component was found in a kit with a later expiration date, leading to incorrect lot and expiration labeling.
Avid Medical is recalling 20 Pediatric Kidney Biopsy Trays because they contain a latex dressing that was not labeled as such.
Avid Medical is recalling 200 custom procedure trays that included latex-containing Telfa dressings without latex warnings. The products were distributed to Virginia and Massachusetts.
Avid Medical is recalling 240 MOHS procedure kits that included a latex-containing dressing without proper labeling.
Avid Medical is recalling 240 MOHS procedure trays because they contained a latex dressing that was not labeled as such.