Cardinal Health 200, LLC recalls Procedure packs: (1) Presource PBDS Cat. PN33BPCR2, Kit, Back, Sterile; (2) Presource PBDS Cat. POCGANA11, Kit, ARN Anterior Hip,…
XXX
Read the official notice →- Date
- 2023-10-18
- Country
- United States
- Brand
- Cardinal Health
- Product
- Procedure packs: (1) Presource PBDS Cat. PN33BPCR2, Kit, Back, Sterile; (2) Presource PBDS Cat. POCGANA11, Kit, ARN Anterior Hip, Sterile;…
- Classification
- Class II
- Units
- Worldwide distribution - US Nationwide distribution in the states of AZ, CA,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2023-11-29
US
Cardinal Health Inc. recalls LEADER brand Dry Eye Relief (Polyethylene Glycol 400, 0.4% Propylene Glycol, 0.3%); 0.33 FL OZ (10 mL) dropper bottle, Sterile,…
Non-Sterility: FDA found insanitary conditions and positive bacterial test results from environmental sampling at the manufacturing facility.
- 2023-11-01
US
Cardinal Health 200, LLC recalls Monoject 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack
Demonstrated recognition and compatibility issues with syringe infusion pumps.
FDA · DeviceCardinal Health 200, LLCUS Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID,…Official notice →- 2023-10-25
US
Cardinal Health 200, LLC recalls Monoject(TM) 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack, Model Number/Product Code: 1180100777
Syringe contains conical tip that is not compatible with certain needleless IV connector(s).
FDA · DeviceCardinal Health 200, LLCNationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL,…Official notice →- 2023-10-18
US
Cardinal Health 200, LLC recalls Procedure pack: Presource PBDS Cat. PLMHCSBHF, Hermann Hospital MHHS, Kit, C Section B MHHS, Sterile.
Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
FDA · DeviceCardinal Health 200, LLCWorldwide distribution - US Nationwide distribution in the states of AZ, CA,…Official notice →- 2023-07-26
US
Cardinal 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.
Other drugs & medical recalls in the United States
- 2023-10-18
US
Ansell Healthcare Products LLC recalls NOVAPLUS GAMMEX NON-LATEX PI GREEN Surgical gloves, REF: V20685255 through V20685290
Some surgical glove sterile pouches were not completely sealed.
FDA · DeviceAnsell Healthcare Products LLCWorldwide - US Nationwide distribution in the states of IN, OH, NY, VA, IL,…Official notice →US
Advance-Esthetic LLC recalls MED-810A Zemits NDPrime Laser products
Advance-Esthetic LLC failed to comply with the applicable standards regarding Electronic Product Radiation Control (EPRC) regulations associated with the laser product performance standards and certification. This…
US
CareFusion 303, Inc. recalls BD Pyxis CII Safe ES, REF: 1116-00; and BD Pyxis : CII Safe ES Desktop PC, Wired SCNR, REF: 107-254-01; CII Safe ES Desktop PC, W-LESS…
When global edit is used to update multiple formulary properties simultaneously, the following properties: 1) Require Lot Number on Recall, 2) Access Destruction Bin (Witness), 3) Add to Destruction Bin (Count/Empty),…
FDA · DeviceCareFusion 303, Inc.US Nationwide distribution in the states of LA, NC, NY, MI, MA, NV, KS, IA, CA.Official notice →US
Cardinal Health 200, LLC recalls Procedure pack: Presource PBDS Cat. PLMHCSBHF, Hermann Hospital MHHS, Kit, C Section B MHHS, Sterile.
Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
FDA · DeviceCardinal Health 200, LLCWorldwide distribution - US Nationwide distribution in the states of AZ, CA,…Official notice →US
RoyalVibe Health Ltd. recalls CellQuicken Analyzer (Smart-Watch and Software), RoyalVibe Ultrasound Generator, Brainvibe, Envirovibe Water Restructuring Pad, RoyalVibe…
Ultrasound devices were not authorized, cleared, or approved by FDA, and thus their performance characteristics have not been adequately established. There is a possibility of customers' reliance on marketing claims…
FDA · DeviceRoyalVibe Health Ltd.US: MI, PA, TX, GA, OH, CA, FL, NY, NH, UT, AL, WA. WI, MN, MA, NM, IA, MD,…Official notice →US
Smiths Medical ASD Inc. recalls Medfusion Syringe Pump, Model 3500-500, v3, v4, v5, and v6
A force sensor in the occlusion detector may drift out of calibration leading to increased occlusion detection times, false occlusion alarms, or a System Failure Alarm. If the force sensor calibration shift is large…
FDA · DeviceSmiths Medical ASD Inc.Worldwide distribution - US Nationwide and the country of Canada.Official notice →