Cardinal Health 200, LLC recalls CardinalHealth Curity Flexible Adhesive Bandage X-Large 2 x 3.75 in. (5.1 x 9.5 cm), Model 44102, Sterile, Hypoallergenic.
Potential contamination of the product with latex adhesive residual.
Read the official notice →- Date
- 2024-05-22
- Country
- United States
- Brand
- Cardinal Health
- Product
- CardinalHealth Curity Flexible Adhesive Bandage X-Large 2 x 3.75 in. (5.1 x 9.5 cm), Model 44102, Sterile, Hypoallergenic.
- Classification
- Class II
- Units
- US Nationwide distribution.
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Cardinal Health recalls
- 2024-11-20
USCardinal Health 200, LLC recalls Monoject U-100 1 mL Insulin Syringe Luer-Lock with Tip Cap Soft Pack, REF 1188100777
Certain lots of listed lots of Cardinal Health Monoject U-100 1 mL Insulin Syringe Luer-Lock with Tip Cap Soft Pack have demonstrated incompatibility with needleless Intravenous (IV) connectors. Cardinal Health…
- 2024-10-02
- US
Cardinal Health 200, LLC recalls (a) CardinalHealth Salem Sump Dual Lumen Stomach Tube with Anti-Reflux Valve, 12 Fr/Ch (4.0 mm) x 48 in. (122 cm), Model #8888266114,…
The firm received reports of breakage in the Anti-Reflux Valve (ARV) due to improper use. As a result, changes to labeling were made.
FDA · DeviceCardinal Health 200, LLCDistribution was nationwide, including Puerto Rico and Guam. There was also…Official notice → - 2024-07-17
- US
Cardinal Health 200, LLC recalls Presource kits and trays, labeled as: 1) Cardiovascular Procedure Kit, Catalog Number SAN29ANCC3; 2) Cardiovascular Procedure Kit,…
Cardinal Health is following the FDA's recommendations regarding the disposition of affected Jiangsu Shenli Medical Production Co. Ltd (Shenli) Syringes in the Merit Medical¿ supplied finished kits. Merit Medical¿…
- 2024-05-08
- US
Cardinal Health 200, LLC recalls Jackson-Pratt 3-Spring Reservoir Kit with PVC Round Drain, 400mL, 7Fr., REF SU130-401D
Cardinal Health is issuing a lot number specific voluntary removal of Jackson-Pratt 3-Spring Reservoir kits due to specific products being shipped to users before undergoing sterilization.
FDA · DeviceCardinal Health 200, LLCWorldwide distribution - US Nationwide and the countries of Panama, Guatemala,…Official notice → - 2024-02-28
- US
Cardinal Health 200, LLC recalls Dover" IRRIGATION 1200 CC TRAY, 60 CC PISTON SYRINGE, STERILE SALINE, TIP PROTECTOR, ALCOHOL, LIDDED
Convenience kits were manufactured and distributed with components which were subsequently recalled by Nurse Assist.
- 2024-02-14
- US
Cardinal Health 200, LLC recalls Cardinal Health Monoject, 1 mL Purple Enteral Syringe with Enfit Connection Sterile, REF 401SE
Cardinal Health is expanding their previous product correction actions to a product removal of all sizes of Cardinal Health brand Monoject sterile Syringe Luer-Lock (1, 3, 6, 12, 20, 35, and 60 mL) and Cardinal Health…
FDA · DeviceCardinal Health 200, LLCDistribution US nationwide and Canada. Foreign distribution updated 9/6/2024…Official notice →
Other drugs & medical recalls in the United States
- 2024-05-29
- US
Dr. Reddy's Laboratories, Inc. recalls Sirolimus Tablets 1mg Tablets 100-count bottle, Rx Only, Distributed by: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made…
Failed Impurities/Degradation Specifications
- US
- US
SUN PHARMACEUTICAL INDUSTRIES INC recalls Xelpros (latanoprost ophthalmic emulsion) 0.005%, 125mcg/2.5mL, 2.5 mL bottle, Rx only, Manufactured by: Sun Pharmaceutical…
Failed Release Testing: Out of specification for particulate matter test.
- 2024-05-22
- US
Macherey Nagel Gmbh & Co. Kg recalls Reagent Test Strips for Blood, Urobilinogen, Bilirubin, Protein, Nitrite, Ketones, Ascorbic Acid, Glucose, pH, Specific Gravity and…
The reason for the recall is one of the test pads, for the parameter leukocytes, was missing on some of the test strips. The issue was identified by a consumer by way of a Henry Schein Inc. (HSI) customer complaint.…
FDA · DeviceMacherey Nagel Gmbh & Co. KgUS Nationwide distribution in the states of CO, FL, IN, NV, TX.Official notice → - US
Cook Medical Incorporated recalls EchoTip¿ Ultra HD Endoscopic Ultrasound Access Needle, ECHO-HD-19-A, G52012
Devices may contain elevated levels of bacterial endotoxin.
FDA · DeviceCook Medical IncorporatedInternational distribution in the countries of Germany, Netherlands,…Official notice → - US
Maquet Medical Systems USA recalls CARDIOHELP-i System. Blood oxygenation and carbon dioxide removal system.
The firm identified that the measured patient leakage current in some devices significantly exceeded expected levels.
FDA · DeviceMaquet Medical Systems USAUS Nationwide distribution in the states of NJ & TX.Official notice →