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),…
Read the official notice →- Date
- 2023-10-18
- Country
- United States
- Brand
- CareFusion
- Product
- 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…
- Classification
- Class II
- Units
- US Nationwide distribution in the states of LA, NC, NY, MI, MA, NV, KS, IA, 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 Details may be shortened or out of date; the official notice is the authoritative source.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 CareFusion recalls
- 2024-06-05
USCareFusion 303, Inc. recalls BD Pyxis(TM) Anesthesia Station 4000, REF: 338
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
FDA · DeviceCareFusion 303, Inc.Worldwide - US Nationwide distribution including in the states of AK, AL, AR,…Official notice →- 2024-03-13
- US
CareFusion 303, Inc. recalls BD Pyxis: MedStation ES, REF: 323; Anesthesia Station ES, REF: 327; MedStation ES Tower, REF: 352;
Automated dispensing cabinets, running affected software, and Windows 10 operating system may experience the application randomly hang, freeze and/or crash, which may result in delays in medication access, and…
FDA · DeviceCareFusion 303, Inc.Worldwide distribution - US Nationwide distribution including in the states of…Official notice → - 2023-11-15
- US
CareFusion 303, Inc. recalls Alaris PCA Module 8120
Alaris PCA Module 8120, Patient Controlled Analgesia infusion pump: compatible syringes labeling contains syringes that have not been validated.
FDA · DeviceCareFusion 303, Inc.Worldwide Distribution: US (nationwide): AK, AL, AR, AS, AZ, CA, CO, DC, DE,…Official notice → - 2023-10-04
- US
CareFusion 303, Inc. recalls BD Pyxis MedBank MedPass Software, REF: 139088-01
After dispensing a timed dose medication for a patient, the automated dispensing cabinet software may continue to show the already dispensed medication dose is still available for dispense, which could lead to…
- 2023-09-27
- US
CareFusion 213, LLC recalls BD ChloraPrep Clear, 2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA) Sterile Solution, 0.03mL (1 ml) each, 60…
Stability data does not support expiry: Shelf-life of the impacted lots of BD ChloraPrep" Clear 1 mL Applicator cannot be substantiated beyond 12-months although labeled with 36-month expiry. Stability studies indicate…
FDA · DrugCareFusion 213, LLCDistributed nationwide to 100 consignees. Please refer to consignee list.Official notice → - 2023-08-23
- US
Carefusion 2200 Inc recalls Snowden-Pencer MIS DIAMOND-TOUCH CLAMP BOWEL 50 MM JAW 5MM, 32CM, RATCHETED, REF SP90-7045; endoscopic surgical device
Specific lots of the product have the potential to exhibit cracking or breaking of the rotation knob due to the incorrect use of an adhesive in the manufacturing process.
Other drugs & medical recalls in the United States
- 2023-10-18
- US
Encore Medical, LP recalls REVERSE PROSTHESIS SHOULDER SYSTEM, SCREW, LOCKING BONE, RSP, 5mmX30mm long, REF: 506-03-130
Reverse shoulder prosthesis package that should contain 5mmx30 screws could contain incorrect 3.5mmx30 screws. Use of incorrect screws could result in surgical delay and inadequate fixation.
FDA · DeviceEncore Medical, LPUS: FL, IN, WI, IA, MN, KY, NY, AZ, RI, WA, OH, SC, VA, TX. OUS: MXOfficial notice → - 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
Cardinal Health 200, LLC recalls Procedure packs: (1) Presource PBDS Cat. PN33BPCR2, Kit, Back, Sterile; (2) Presource PBDS Cat. POCGANA11, Kit, ARN Anterior Hip,…
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FDA · DeviceCardinal Health 200, LLCWorldwide distribution - US Nationwide distribution in the states of AZ, 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 →