Cardinal Health 200, LLC recalls Cardinal Health Jackson-Pratt Channel Drain, 32 Fr, REF JP-2292
Cardinal Health recently received multiple complaints regarding various performance issues with Cardinal Health Jackson-Pratt Channel Drains including lack of radiopacity in wound drains, dull trocars impacting product…
Read the official notice →- Date
- 2023-01-25
- Country
- United States
- Brand
- Cardinal Health
- Product
- Cardinal Health Jackson-Pratt Channel Drain, 32 Fr, REF JP-2292
- Classification
- Class II
- Units
- Worldwide distribution - US Nationwide and the countries of Canada, Saudi…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2023-07-26
USCardinal Health 200, LLC recalls NovaPlus Infant Heel Warmer, Instant Squeeze Activation, Catalog Number V11460-010
Cardinal Health has received an increase in burst/leaking complaints from mid-April to May regarding the above listed lot of the Novalplus Infant Heel Warmer with tape.
- 2023-06-14
- US
Cardinal Health 200, LLC recalls Presource Kit, SMA21LPUHJ GYN Laparoscopy Pack. Convenience kit used for Laparoscopic surgery
Inadvertently released for distibution without sterility assurance.
- 2023-03-01
- US
Cardinal Health 200, LLC recalls Cardinal Health Presource Packs IV START TRAY I-Intended for IV access device CATALOG #: 01-5799A
Presource Kits contains the ICU MicroClave Clear Connector due to a manufacturing defect there is a gap between the connectors top and bottom housings which may lead to fluid leaks and loss of fluid path integrity
FDA · DeviceCardinal Health 200, LLCUS Nationwide distribution in the states of GA, PA.Official notice → - 2022-12-14
- US
Cardinal Health recalls Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 ml) 5ml Catheter Product Code: 2480 Intended for urinary drainage from the…
Occlusion (blockage) of the bubble inlet port of the urinary drainage bag which may prevent urine draining into the bag. If the bladder is not emptied within a clinically appropriate time, this may increase the risk of…
- 2022-11-16
- US
Cardinal Health 200, LLC recalls Cardinal Health GEL PACK REUSABLE, SMALL, Cat. 70204
Users are being informed that the product should not be used on infants/neonates. A caution statement will be added to the labeling stating: Not for use on Infants/Neonates .
- 2022-05-25
- US
Cardinal Health Inc. recalls Trulicity (dulaglutide) injection, 0.75 mg/0.5mL once weekly, 4 Single-Dose Pens, Rx only, Eli Lilly and Company, Indianapolis, IN 46285,…
TEMPERATURE ABUSE: Products were exposed to temperatures outside of the products labeled storage conditions
Other drugs & medical recalls in the United States
- 2023-01-25
- US
R & D Systems, Inc. recalls R&D CBC-3D Hematology Control: (1) CBC-3D Normal Pack Hematology Control, REF 3D501, containing 10 x 2.0mL Control N; (2) CBC-3D TRI PACK…
For one lot of CBC-3D Hematology Control, the Normal Level may exhibit hemolysis or deterioration due to microbial contamination.
FDA · DeviceR & D Systems, Inc.Worldwide distribution - US Nationwide distribution in the states of CA, FL,…Official notice → - US
Bolton Medical Inc. recalls RELAY PRO, THORACIC STENT-GRAFT SYSTEM, REF 28-M4-XX-XXX-XXX
The product may be shorter than packaging indicates
FDA · DeviceBolton Medical Inc.Worldwide distribution - US Nationwide and the countries of UK, France,…Official notice → - US
Maquet Cardiovascular, LLC recalls Vasoshield Syringe Packs, Model VH-5001
Ink on the Vasoshield syringe Maquet logo may chip resulting in an unreasonable risk of harm to the patient. Potential harms may include foreign body reaction, coronary embolic event, and peripheral embolic event.
- US
Abbott Laboratories recalls Alinity Reaction Vessels, REF: 06P1401, for use with Alinity i Systems; ARCHITECT Reaction Vessels
Reaction vessels may contain a potential contaminant that could affect their optical performance.
FDA · DeviceAbbott LaboratoriesUS Distribution: IL, MN, MO, NC, ND, NJ, NY, OK, SC, TX, WVOfficial notice → - US
Mobius Imaging, LLC recalls MobiCT-32 AIRO Mobile CT Scanner, Cat. No. MobiCT-32, mobile computed tomography system.
Stryker received one report of an injury to an untrained user that occurred while the untrained user was moving an Airo TruCT unit in reverse. The firm will increase visibility of instructions for users to consider…
FDA · DeviceMobius Imaging, LLCWorldwide distribution - US Nationwide and the countries of Algeria,…Official notice → - US
Siemens Medical Solutions USA, Inc recalls ARTIS pheno, ARTIS icono biplane, and ARTIS icono floor
Mechanical connection between the tabletop and table base may be lost.
FDA · DeviceSiemens Medical Solutions USA, IncWorldwide distribution - US Nationwide and the countries of Armenia,…Official notice →