Drugs & medicalClass II

Smiths Medical ASD Inc. recalls smiths medical medex CBSS-5ML, Triple set, (172/15cm), Model Number DPSHC0092

Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets.

Read the official notice →
Date
2021-10-20
Country
United States
Brand
Smiths Medical ASD
Product
smiths medical medex CBSS-5ML, Triple set, (172/15cm), Model Number DPSHC0092
Classification
Class II
Units
Austria, France, Germany, Great Britain, and Saudi Arabia
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 Details may be shortened or out of date; the official notice is the authoritative source.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

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. 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 Smiths Medical ASD recalls

  1. 2021-11-03
  2. US
    Drugs & medicalClass II

    Smiths Medical ASD Inc. recalls Bivona Aire-Cuf Endotracheal Tube

    Inadequate pouch seal leading to a compromised sterile barrier on products with a shaft length of 325mm.

    FDA · DeviceSmiths Medical ASD Inc.Worldwide distribution - US Nationwide distribution in the states of AL, AZ,…Official notice →
  3. US
    Drugs & medicalClass III

    Smiths Medical ASD Inc. recalls Pneupac paraPac plus 300 ventilator kit, REF P300NGB

    Two devices were labeled with the same serial number

    FDA · DeviceSmiths Medical ASD Inc.UKOfficial notice →
  4. 2021-10-27
  5. US
    Drugs & medicalClass II

    Smiths Medical ASD Inc. recalls medfusion Stopcock, 1-way and 4-way, Model Numbers (REF): a. 081-101BE b. 081-101GE c. 081-101GEE d. 081-101NE e. 081-102NE f. 081-102RE…

    Product has a lack of sterility assurance

    FDA · DeviceSmiths Medical ASD Inc.International Distribution to countries of: Armenia, Austria, Germany, Great…Official notice →
  6. US
    Drugs & medicalClass II

    Smiths Medical ASD Inc. recalls smiths medical portex Loss of Resistance Device, REF 100/398/000

    The labeling was missing information on sterilization and prohibition of reuse.

    FDA · DeviceSmiths Medical ASD Inc.Canada. Belgium, Great Britain, Ireland, Czech Republic, Spain, France,…Official notice →
  7. US
    Drugs & medicalClass II

    Smiths Medical ASD Inc. recalls CADD Administration Sets, Model #21-7346-24

    Product may have been manufactured with an air filter assembled in an incorrect orientation.

    FDA · DeviceSmiths Medical ASD Inc.CanadaOfficial notice →
  8. US
    Drugs & medicalClass I

    Smiths Medical ASD Inc. recalls CADD-Solis VIP ambulatory infusion pump, Model Numbers: a. 21-2120-0105-02L b. 21-2120-0105-03L c. 21-2120-0105-06L d. 21-2120-0105-07L…

    Specific Pumps may exhibit intermittent performance in the AILD (Air in Line Detector) function. If an AILD does not sufficiently discern fluid from air in line, an air in line event may not be recognized by the pump…

    FDA · DeviceSmiths Medical ASD Inc.Distribution to European countries: BE, BH, CH, DE, DK, ES, FI, FR, GB, IT,…Official notice →
All 39 Smiths Medical ASD recalls →

Other drugs & medical recalls in the United States

  1. 2021-10-20
  2. US
    Drugs & medicalClass II

    Intuitive Surgical, Inc. recalls Ion Flexison Biopsy Needle, 19G, Extension Range : 0-3 cm, Ref: 490104-09 and 49004-10, 5-pack, Sterile EO, Rx only, UDI:00886874115978

    Potential for the sheath tip on the biopsy needle to separate from the sheath shaft.

    FDA · DeviceIntuitive Surgical, Inc.US: AZ, AR, CA, CO, DC, FL, GA, IL, IN, IO, MD, MA, MI, MN, MO, NV, NJ, NY,…Official notice →
  3. US
    Drugs & medicalClass II

    Centese Inc. recalls Thoraguard Chest Tube Kit, 20 Fr

    An adhesive joint in the SmartValve component of the device can become compromised resulting in a leak.

    FDA · DeviceCentese Inc.Distribution to a single consignee located in California.Official notice →
  4. US
    Drugs & medicalClass II

    K2M, Inc recalls Chesapeake Anterior Lumbar (AL) Removal Tool; Cat. no. 2008-90068

    Units may arrive with missing pins and/or in a state in disassembly. Pins dislodging from the instrument during a procedure may enter the surgical cavity, requiring intraoperative removal or revision surgery.

    FDA · DeviceK2M, IncDomestic distribution to CO, IL, LA, MA, MS, OK, PA, TN, and TX. Foreign…Official notice →
  5. US
    Drugs & medicalClass I

    Red Medical Supplies recalls EcoGel 200 - RED Medical Supplies Blue Ultrasound Gel, Model No. 250UG-BMU

    Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. On August 18, 2021,FDA published a Letter to Health Care Providers to further address this issue:…

    FDA · DeviceRed Medical SuppliesFirm sold product through Amazon.com. Domestic distribution nationwide.Official notice →
  6. US
    Drugs & medicalClass II

    Inpeco S.A. recalls FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2). (Different brand names of same product.)

    The Firmware (FW) of the Automation System Interface Module to ADVIA Centaur XP/XPT may lead to an incorrect association of test results to sample ID. Improper management of the sample may bring an incorrect patient…

    FDA · DeviceInpeco S.A.Domestic distribution nationwide . Foreign distribution worldwide.Official notice →
  7. US
    Drugs & medicalClass II

    Medtronic Sofamor Danek USA Inc recalls Endoskeleton" TCS Interbody System with Titan nanoLOCK" Surface Technology, NanoLock, 6 Deg, Interbody, Medium, 10mm

    Engraving on implants may not match what is listed on the pouch labels.

    FDA · DeviceMedtronic Sofamor Danek USA IncDistribution in US: CA, MN, MO, NC, NV, NY, OH, OK, OR, PA, SC, SD, WA, WVOfficial notice →
See all drugs & medical recalls →