Drugs & medicalClass II

Quest Medical, Inc. recalls Precision Delivery Set with Filter, REF: PD06F; and Precision Delivery Set with Trifurcated Luer, REF: PDT05CV2

Delivery Sets may have tubing that could become detached that could result in patient infection.

Read the official notice →
Date
2023-02-15
Country
United States
Brand
Quest Medical
Product
Precision Delivery Set with Filter, REF: PD06F; and Precision Delivery Set with Trifurcated Luer, REF: PDT05CV2
Classification
Class II
Units
US Nationwide distribution in the state of MA.
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Quest Medical recalls

  1. 2023-11-08
  2. US
    Drugs & medicalClass II

    Quest Medical, Inc. recalls Q2 Multiport Extension set, REF: 9520, Rx Only Sterile, single use non-pyrogenic intravenous fluid administration sets with a multiport IV…

    For administration of intravenous fluids to a patient s vascular system utilizing needle-free components and I.V. manifold for multiple simultaneous intravenous therapy via gravity, syringe, or infusion pump. Use of a…

    FDA · DeviceQuest Medical, Inc.US:TX, UT, FL, CA, VA, CO, AL, NV, IL, OK, OH, PA, MO, MN, MT, WA, MI, TN, NY…Official notice →
All 2 Quest Medical recalls →

Other drugs & medical recalls in the United States

  1. 2023-02-15
  2. US
    Drugs & medicalClass II

    Olympus Corporation of the Americas recalls SPiN Thoracic Navigation System Model: SYS-4000 (SYS-4000D)

    A grainy image is observed when using a SPiN Vision Single-Use Flexible Bronchoscope (models INS-7100 or INS-7130) with the SYS-4000 system due to an incorrect DVI cable supplied may result in prolonged…

    FDA · DeviceOlympus Corporation of the AmericasFL, GA, IN, MD, MS, NY, OH, PA, RI, SC, VAOfficial notice →
  3. US
    Drugs & medicalClass II

    Wishbone Medical, Inc. recalls WishBone Medical Smart Correction Dual Joint Express Struts, external skeleton fixation device Type Part Number XXS 10-702-080095-0 XS…

    Firm identified that user may be unable to adjust the length of the Smart Correction Dual Joint Express Struts due to the collar release pin backing out. This may lead to a delay in correction.

    FDA · DeviceWishbone Medical, Inc.US Nationwide distribution in the state of South Carolina.Official notice →
  4. US
    Drugs & medicalClass II

    TriMed Inc. recalls RipCord Syndesmosis Button, REF: STA001K

    Overly aggressive tension on the pull suture, while passing the medial button through a bone/soft tissue tunnel across the fibula and tibia, can exceed its strength causing it to break.

    FDA · DeviceTriMed Inc.US Nationwide distribution in the states of IL, PA, TX, GA, TN, AL, MO, FL,…Official notice →
  5. US
    Drugs & medicalClass II

    TEKNIMED SAS recalls HIGH V+ Spinal Cement System REF T040321K

    Incorrect expiry date. Product is labeled with expiry date 2027-02-28. The correct expiration date is 2025-02-28.

    FDA · DeviceTEKNIMED SASWorldwide distribution - U.S. Nationwide distribution in the state of MS and…Official notice →
  6. US
    Drugs & medicalClass II

    Zimmer, Inc. recalls Identity Shoulder System Resection Planer 35mm Resection Planer

    Two planers were found to be unusable during sawbones shoulder training.

    FDA · DeviceZimmer, Inc.US Nationwide distribution in the states of AR, CA, IL, MI, NJ, NY, OK, PA,…Official notice →
  7. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls Sterile Procedural Trays, labeled as the following: a. BREAST AUGMENTATION b. BREAST REDUCTION CDS c. CUH ABDOMINOPLASTY CDS…

    Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldWorldwide distribution - US Nationwide and the countries of Canada, Japan,…Official notice →
See all drugs & medical recalls →