Manufacturer
115 recalls in our database name AVID Medical, Inc. as the manufacturing or recalling firm.
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 574 General Laparoscopy Trays due to inadvertent resterilization causing discoloration of the CLEARIFY VISUALIZATION SYSTEM. The discoloration could compromise surgical visibility.
AVID Medical is recalling the CARDIAC ROBOT PACK medical convenience kit after inadvertent resterilization caused discoloration of the visualization system. Twenty units distributed across seven U.S. states are affected.
AVID Medical is recalling laparoscopic trays because the visualization system became discolored from inadvertent resterilization. Forty units were distributed to healthcare facilities in CA, IL, MD, OH, PA, TX, and WA.
AVID Medical is recalling GENERAL ROBOTIC PACK medical kits due to discoloration of the CLEARIFY VISUALIZATION SYSTEM caused by inadvertent resterilization. A total of 203 units were distributed across seven states.
AVID Medical is recalling 372 Robotic Uro/Gyn Packs in which the visualization system was inadvertently resterilized, causing discoloration. Affected products were distributed domestically in California, Illinois, Maryland, Ohio, Pennsylvania, Texas, and Washington.
AVID Medical's GYN ROBOTIC PACK medical convenience kits have been recalled due to inadvertent resterilization causing discoloration of the visualization system. The recall affects 45 units distributed in six states.
AVID Medical is recalling 292 LAVH Pack surgical kits due to inadvertent resterilization that caused discoloration of the CLEARIFY VISUALIZATION SYSTEM. Affected kits were distributed in seven U.S. states.
AVID Medical, Inc. is recalling 321 units of GEN LAPAROSCOPY PACK kits distributed in six states due to discoloration of the visualization system caused by inadvertent resterilization.
AVID Medical is recalling the GS Endoscopy Pack due to inadvertent resterilization that caused discoloration of the visualization system. The recall affects 816 units distributed across seven states.
AVID Medical is recalling Partial Nephrectomy Packs (52 units) because the CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized, causing discoloration.
AVID Medical is recalling 46 robotic partial nephrectomy surgery kits due to inadvertent re-sterilization of the visualization system component, which caused discoloration.
AVID Medical recalls HVI Cardiac Robot Pack medical kits due to inadvertent resterilization of the CLEARIFY Visualization System, causing discoloration. No injuries reported.
AVID Medical is recalling DAVINCI UROLOGY medical convenience kits because they were inadvertently resterilized, causing discoloration. The recall affects 166 units distributed domestically.
AVID Medical is recalling CT DAVINCI Medical convenience kits that were inadvertently resterilized during manufacturing, causing discoloration. The kits were distributed domestically in seven states.
AVID Medical is recalling ROBOTIC PROSTATECTOMY PACK units due to inadvertent resterilization of the CLEARIFY VISUALIZATION SYSTEM, which caused discoloration. The kits were distributed domestically.
AVID Medical is recalling 346 GYN Laparoscopy Packs due to discoloration caused by inadvertent resterilization. Affected kits were distributed in seven states.
AVID Medical is recalling 626 DAVINCI TRUCUSTOM BUNDLE medical kits because the CLEARIFY VISUALIZATION SYSTEM was inadvertently re-sterilized, causing discoloration. Affected units were distributed in CA, IL, MD, OH, PA, TX, and WA.
AVID Medical is recalling 656 PACK GENERAL ROBOTIC medical convenience kits that were inadvertently resterilized, causing discoloration. The defective kits were distributed in California, Illinois, Maryland, Ohio, Pennsylvania, Texas, and Washington.
AVID Medical is recalling laparoscopic gynecology kits due to improper resterilization that caused discoloration. The recall affects 18 units distributed across several states.
AVID Medical recalled the LAP CHOLE PACK surgical kit after the CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized, causing discoloration of the device.
AVID Medical is recalling Halyard RAPIDES E-PACK Cardiovascular Procedure Kits due to a coating defect on surgical needles that may diminish needle performance during procedures. The defect affects units distributed nationwide in Illinois and Louisiana.
AVID Medical is recalling Halyard SUTURE PACK CABG cardiovascular surgical kits due to a raw material defect in the silicone coating of surgical needles. The coating may diminish or detach during use, potentially affecting suture performance.
AVID Medical is recalling Halyard CHRIST SUTURE KIT due to coating issues on surgical needles that may degrade during use. The defect could affect device performance in surgical procedures.
AVID Medical is recalling Halyard PACEMAKER PK medical convenience kits because sponge forceps and towel clamps may shed loose metal flakes that could enter a patient's surgical site, causing local or foreign body reactions.
AVID Medical recalls Halyard D & C surgical convenience kits due to potential metal flakes that could detach from forceps and clamps. Affected lot 1596759 was distributed nationwide.