Drugs & medicalClass II

Collagen Matrix, Inc. recalls DuraMatrix-Onlay Collagen Dura Substitute Membrane 4 inches x 5 inches (10.0cm x 12.5cm) REF: CDSLM45

Outer packaging (outer pouch) is not sealed compromising sterility and result in potential risk of patient infection, which could lead to revision surgery

Read the official notice →
Date
2022-03-02
Country
United States
Brand
Collagen Matrix
Product
DuraMatrix-Onlay Collagen Dura Substitute Membrane 4 inches x 5 inches (10.0cm x 12.5cm) REF: CDSLM45
Classification
Class II
Units
DuraMatrix-Onlay distributed US Nationwide in the states of FL, IN, Puerto…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Collagen Matrix recalls

  1. 2022-10-05
  2. US
    Drugs & medicalClass II

    Collagen Matrix Inc recalls Collagen Dental Wound Dressing - Bovine Dermis Tap, 25mm x 75mm Product was distributed under the following brand names: 1) Cytoplast…

    The packaging may not be sealed, which could compromise sterility.

    FDA · DeviceCollagen Matrix IncUS distribution to distributors in IL, IN, MI, NC, OH, and TXOfficial notice →
All 2 Collagen Matrix recalls →

Other drugs & medical recalls in the United States

  1. 2022-03-09
  2. US
  3. 2022-03-02
  4. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls meridian bioscience immunocard STAT! Rotavirus test, REF 750030, 30 tests/kit box. The ImmunoCard STAT! Rotavirus…

    The product was incorrectly shipped at room temperature rather than refrigerated.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Distribution was made to IL, FL, LA, MS, NC, OH, and TX.Official notice →
  5. US
    Drugs & medicalClass II

    Biomet, Inc. recalls Comprehensive Shoulder System Primary Shoulder Stem, Micro Length, Porous Plasma, 11 MM, 55 MM Long Item Number: 113611

    The products in scope underwent an incorrect rework operation for the porous plasma sprayed coating. Internal testing indicated that the parts may not have sufficient adhesion strength. The scope was identified to be…

    FDA · DeviceBiomet, Inc.Worldwide distribution - US Nationwide and the countries of Canada, Ecuador,…Official notice →
  6. US
    Drugs & medicalClass II

    C.R. Bard Inc recalls BARD SURESTEP INTERMITTENT CATHETER TRAY, 14Fr, REF INTS14C

    There is a potential to leak from the catheter where it connects to the drain bag

    FDA · DeviceC.R. Bard IncUS Nationwide distribution in the states of GA, ME, NJ, WI, MN, SD, CO, ND,…Official notice →
  7. US
    Drugs & medicalClass III

    Becton Dickinson & Company recalls BD Vacutainer Luer Lok Access Device - intended as a sterile, single use device designed to provide a connection to a catheter port…

    May shed contaminant particles into the urine specimen that may be misidentified as Red Blood Cells when used in conjunction with the Sysmex UF-1000i or UX-2000 Analyzers and lead to false elevations in RBC counts

    FDA · DeviceBecton Dickinson & CompanyUS Nationwide distribution in the state of IL.Official notice →
  8. US
    Drugs & medicalClass II

    Stryker Sustainability Solutions recalls REF: 5921-018-135, Stryker Color Cuff, 18" (Red), Quick Connect Single Port, Single Bladder

    Mislabeling; dual-bladder tourniquet cuffs are labeled as single-bladder inflatable cuffs.

    FDA · DeviceStryker Sustainability SolutionsUS: KS OK TX OUS: NoneOfficial notice →
See all drugs & medical recalls →