Manufacturer
152 recalls in our database name Centurion Medical Products Corporation as the manufacturing or recalling firm.
Of the 152 recalls from Centurion Medical Products Corporation we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2 (1%) 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.
Centurion Medical Products is recalling specific biopsy trays because incomplete sterile package seals may compromise sterility.
Centurion Medical Products is recalling specific Incision and Drainage Trays because incomplete seals may compromise sterility.
Centurion Medical Products Corporation is recalling Debridement Trays because incomplete seals on the sterile package may compromise sterility.
Centurion Medical Products is recalling Suture Trays because incomplete seals on the sterile package may compromise sterility.
Centurion Medical Products Corporation is recalling blood culture collection kits due to incomplete seals that may compromise sterility.
Centurion Medical Products is recalling 30 Nosebleed Tray kits (Kit Code MNS3885) distributed in Connecticut and Illinois because they contain Major Nasal Decongestant Spray.
Centurion Medical Products Corporation is recalling 644 YNHH Scope Kits because they contain Major Nasal Decongestant Spray. The kits were distributed in Connecticut and Illinois.
Centurion Medical Products is recalling 525 Epistaxis Tray Kits because they contain major nasal decongestant spray.
Centurion Medical Products is recalling 80 units of Universal Line Full Body Drape Kits due to incomplete sterile packaging seals that may compromise product sterility.
Centurion Medical Products Corporation is recalling 11,260 Port Access Kits distributed in Illinois. The recall was initiated by the supplier due to an issue with GRIPPER Needles.
Centurion Medical Products Corporation is recalling GRIPPER Needles in Illinois. The recall was initiated by the supplier.
Centurion Medical Products Corporation is recalling 200 Port Access Infusion Kits with 1-inch needles distributed in Illinois due to a supplier-initiated recall.
Centurion Medical Products Corporation is recalling 240 Port Full Access Tray kits in Illinois due to a supplier-initiated recall of GRIPPER Needles.
Centurion Medical Products is recalling Central Line Bundles containing BD MaxZeroNeedleess Connectors due to a risk of fluid droplets separating from the sealed surface.
Centurion Medical Products is recalling IV Securement Kits containing a recalled BD connector due to the potential for fluid droplets to separate from the sealed surface.
Centurion Medical Products Corporation is recalling Sorbaview IV kits because the included BD MaxZeroNeedleess Connector may release fluid droplets after disconnection.
Centurion Medical Products Corporation is recalling Infusa Port Kits containing a specific connector due to the potential for fluid droplets to separate from the sealed surface.
Centurion Medical Products is recalling CAP Bundle Kits because the included BD MaxZeroNeedleess Connector may release fluid droplets after disconnection.
Centurion Medical Products is recalling CVC Triple Lumen Safety Bundles because the included BD MaxZeroNeedleess Connector may leak fluid droplets after disconnection.
Centurion Medical is recalling central line bundles containing a BD MaxZeroNeedleess Connector due to the potential for fluid droplets to separate from the sealed surface after disconnection.
Centurion Medical Products is recalling CAP CHANGE KIT DYNDC1496B because the included BD MaxZeroNeedleess Connector may release fluid droplets after disconnection.
Centurion Medical Products is recalling 1,530 Circlamps due to a design mismatch that may cause the device to remove foreskin without a scalpel.
Centurion Medical Products Corporation is recalling Central Venous Access Device Bundles because they include a connector recalled for potential fluid droplet separation.
Centurion Medical Products is recalling VANTEX 7FR, 16CM, 3L CVC Bundles because the included BD MaxZeroNeedleess Connector may leak fluid droplets after disconnection.
Centurion Medical Products is recalling IV Start Kits containing a recalled BD connector due to potential fluid droplet separation.