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, Inc. is recalling 30 DAVINCI LAP/GYN kits (Model WRNM037-16) because they may be contaminated with a lubricant used during manufacturing.
AVID Medical, Inc. is recalling 33 Endovascular Packs (Model VAPX014-04) because they may be contaminated with a lubricant used during manufacturing.
AVID Medical, Inc. is recalling 20 Urology Major kits (Model WRNM058-10) because they may be contaminated with a lubricant used during manufacturing.
AVID Medical, Inc. is recalling 96 Heart Prep Trays (Model MECV97W) because they may be contaminated with a lubricant used during manufacturing.
AVID Medical, Inc. is recalling 28 units of EURO053 plastic trays potentially contaminated with manufacturing lubricant. The units were distributed in AZ, CA, FL, MD, NE, and TX.
Avid Medical is recalling 124 Open Heart CFH kits because they may be contaminated with a lubricant used during manufacturing.
Avid Medical, Inc. is recalling 144 Davinci Trucustom Bundles because they may be contaminated with a lubricant used during manufacturing.
AVID Medical, Inc. is recalling 10 Craniotomy Packs (Model WRNM035-20) because they may be contaminated with a lubricant used during manufacturing.
AVID Medical, Inc. is recalling 134 GYN Laparoscopy/Laparotomy kits due to potential contamination with a manufacturing lubricant.
AVID Medical, Inc. is recalling 15 laparoscopic prostatectomy kits because they may be contaminated with a lubricant used during manufacturing.
Avid Medical, Inc. is recalling 59 units of Adult Heart Tray Shands Jacks (Model SHND419-08) because they may be contaminated with a lubricant used during manufacturing.
Avid Medical, Inc. is recalling six Robotic Prostatectomy Packs (NAMC423-11) because they may be contaminated with a manufacturing lubricant.
AVID Medical, Inc. is recalling 40 Major Packs (Model NIHB0018-11) because they may be contaminated with a lubricant used during manufacturing.
AVID Medical, Inc. is recalling 28 GYN Laparoscopy Packs (Model NAMC436-12) because they may be contaminated with a lubricant used during manufacturing.
AVID Medical, Inc. is recalling 23 ABD Hysterectomy kits (Model NAMC438-07) because they may be contaminated with a lubricant used during manufacturing.
AVID Medical is recalling Halyard IV Start Kits because they contain applicators potentially contaminated with Aspergillus penicillioides.
AVID Medical is recalling 192 Halyard IV Start Kits because the included BD ChloraPrep applicators may have open or incomplete packaging seals.
AVID Medical is recalling Halyard IV Start Kits because the included BD ChloraPrep applicators may have open or incomplete packaging seals.
AVID Medical is recalling 1,640 Haylard 18G Single Shot Epi Trays because they contain Sodium Chloride ampules subject to a separate recall for potential quality and sterility issues.
AVID Medical is recalling Haylard Basic Biopsy Trays because they contain Sodium Chloride ampules subject to a separate recall for quality and sterility issues.
AVID Medical is recalling 340 biopsy kits because they contain sodium chloride ampules subject to a separate recall for quality and sterility issues.
AVID Medical is recalling 80 Haylard Continuous Nerve Block Kits due to potential sterility issues in included Sodium Chloride ampules.
AVID Medical is recalling Halyard IV Start Kits because they contain applicators contaminated with Aspergillus penicillioides.
AVID Medical is recalling 98 Halyard IV Start Kits because wrinkles in the paper lidding may breach the seal, compromising sterility assurance.
AVID Medical is recalling specific lots of Halyard medical convenience kits containing Ritmed Neurological Sponges due to potential endotoxin level variability.