Recall archive
18 recalls · page 1 of 1
Reported Jul 15, 2020
Centurion DIFFICULT IV KIT containing BD's Vacutainer Plastic Lithium Heparin Tubes (BD Vacutainer-BD Codes 367884 &…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centurion Medical Products Corporation
Matched: Brand · Product · Product details — False elevation of carboxyhemoglobin (COHb) results in blood samples collected using BD Vacutainer¿ Plastic Lithium Heparin tubes with the IL GEM…
FDA (openFDA device enforcement)
Reported Feb 12, 2020
Centurion Circumsion Trays as follows: Kit Code Product CIT1270 CIRCUMCISION TRAY CIT2365 CIRCUMCISION TRAY CIT2465…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centurion Medical Products Corporation
Matched: Brand · Product · Product details — Incomplete seals on the sterile package may compromise the sterility
53 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2019
EPISTAXIS TRAY Kit Code: MNS10165
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centurion Medical Products Corporation
Matched: Brand · Reason for recall — Various medical device kits contain MAJOR Nasal Decongestant Spray is being recalled by the manufacturer
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Centurion Medical Products UNIVERSAL LINE FULL BODY DRAPE KIT - REG Code: DT11955
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centurion Medical Products Corporation
Matched: Brand · Product · Product details — Sterile packaging incomplete seals may compromise sterility of the product
FDA (openFDA device enforcement)
Reported Nov 6, 2019
Port full Access Tray Product Code: DT19330
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centurion Medical Products Corporation
Matched: Brand — Supplier initiated recall of the GRIPPER Needles
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 16, 2019
PICC Line Accessory Kit CVI4285
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centurion Medical Products Corporation
Matched: Brand — Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of…
34 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2019
STERILE GRAVES VAGINAL SPECULUM MEDIUM Kit Code # GVS10MST - Product Usage:The speculum is used to spread the walls of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centurion Medical Products Corporation
Matched: Brand · Product details — Potential for sterile packaging to be compromised
12 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 7, 2019
Sheridan Endotracheal Tube contained inside Centurion kit code TC7855.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Centurion Medical Products Corporation
Matched: Brand · Product · Product details · Reason for recall — Centurion is conducting a sub-recall for Teleflex Sheridan branded Endotracheal Tracheal Tubes due to increased incidence of Sheridan connector…
FDA (openFDA device enforcement)
Reported Jun 12, 2019
Sterile Nail Clipper Concave Edge (67710)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centurion Medical Products Corporation
Matched: Brand — Compromised seal on the sterile barrier pouch.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 28, 2018
SKIN STAPLE REMOVER
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centurion Medical Products Corporation
Matched: Brand — Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf…
20 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 10, 2018
SafetyGlide Needle, 22GA 1-1/2in, Catalog n. 301701, manufactured by BD, sold in Centurion Convenience Kits. Centurion…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centurion Medical Products Corporation
Matched: Brand · Product · Product details · Reason for recall — Centurion is recalling specific lots of convenience kits, SafetyGlide Needle, 22GA 1-1/2in, manufactured by BD, sold in Centurion Convenience Kits.…
FDA (openFDA device enforcement)
Reported Apr 12, 2017
POST-OP EYE TRAY The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centurion Medical Products Corporation
Matched: Brand · Product details · Reason for recall — Centurion Medical Products is recalling Convenience Kits that contain Covidien Curity Oval Eye Pads due to supplier's recall because of potential…
6 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 14, 2016
Multi-Med Single Lumen Catheters sold in Centurion convenience kits. The Multi-Med catheter is indicated for use in…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Centurion Medical Products Corporation
Matched: Brand · Product · Product details — The kits contain Multi-Med Single Lumen Catheters that have a potential for excess material to remain at the tip of the catheter from the…
FDA (openFDA device enforcement)
Reported Jul 27, 2016
Convenience Kits from Centurion that contain a Medtronic/Covidien Light Glove ED SUTURE KIT VAGINAL DELIVERY TRAY…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centurion Medical Products Corporation
Matched: Brand · Product · Product details · Reason for recall — Kits from Centurion contain a Medtronic/Covidien Light Glove that is being recalled by the manufacturer, Medtronic. According to the notice received…
FDA (openFDA device enforcement)
Reported Mar 2, 2016
Convenience Kits from Centurion that contain an In-Vision- Plus Needleless IV Connector, Model: code RYM5001…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centurion Medical Products Corporation
Matched: Brand · Product · Product details — Convenience Kits contain an In-Vision-Plus Needleless IV Connector, code RYM5001 that is being recalled by the manufacturer, RyMed Technologies, LLC.…
FDA (openFDA device enforcement)
Reported Jan 14, 2015
Chest Tube Tray (Cardiovascular Surgical Instruments convenience kit)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centurion Medical Products Corporation
Matched: Brand — According to the recall notice received from Hospira, the recall was initiated due to a confirmed customer report of particulate in a single unit.…
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 1, 2014
0.9% Sodium Chloride Injection, USP BD PosiFlush(TM) SF Saline Flush Syringe 10 mL REF#306553 used in Centurion…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centurion Medical Products Corporation
Matched: Brand · Product · Product details — Unit packages may exhibit open seals which impacts package integrity and potentially product sterility.
FDA (openFDA device enforcement)
Reported Dec 18, 2013
Centurion Sterile # 84 Rubber Bands Reorder EB84, Caution: This product contains natural rubber latex which may cause…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centurion Medical Products Corporation
Matched: Brand · Product · Product details — Package labeling indicates both "latex free" and "contains natural rubber latex" . The rubber bands do contain natural rubber latex. This could cause…
FDA (openFDA device enforcement)
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