Drugs & medicalClass II

MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE STERILE IRIS SCISSORS CVD/STD, REF DYNJ04049

4.5" Iris Scissors, Sterile, Curved (DYNJ04049) are being recalled due to the potential of the tip protector to fall off. The sharp tip of the scissors could compromise the sterile barrier system by puncturing large…

Read the official notice →
Date
2023-09-27
Country
United States
Brand
MEDLINE INDUSTRIES, LP - Northfield
Product
MEDLINE STERILE IRIS SCISSORS CVD/STD, REF DYNJ04049
Classification
Class II
Units
Worldwide distribution: US (nationwide) and OUS (foreign) countries of:…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 MEDLINE INDUSTRIES, LP - Northfield recalls

  1. 2023-11-15
  2. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls Clinical TREAT Antifungal Powder, Vanilla Scent, 3 OZ (85 g) tube, Active Ingredient: Miconazole Nitrate 2.0% w/w…

    CGMP deviations: the product was shipped from the Manufacturer to a Medline warehouse and released to stock while it was still under investigation for low assay results on the active ingredient miconazole nitrate.

    FDA · DrugMEDLINE INDUSTRIES, LP - NorthfieldNationwideOfficial notice →
  3. 2023-10-25
  4. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE ReNewal Harmonic ACE+7 Shears w/ Adv. Hemostasis Use Only w/ GEN11 SW v2018-1 and Lower, REF HARH45R. surgical…

    Various reprocessed Covidien LigaSure and Ethicon Harmonic devices may have an incomplete seal on the packaging tray.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUSOfficial notice →
  5. 2023-10-11
  6. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls Centurion Sterile CirClamp with 1.45cm Bell Reprocessed, Reorder CR3145K, 1 per package, 12 per case.

    The kits incorrectly contain CirClamp subassembly 345CRSAK which results in the kits containing an incorrect bell and base size.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution.Official notice →
  7. 2023-09-20
  8. US
    Drugs & medicalClass I

    MEDLINE INDUSTRIES, LP - Northfield recalls HUDSON RCI Addipak, UNIT DOSE VIALS, 5mL Sterile 0.9% NaCl Solution for Inhalation USP. REF RHUD59U

    Product dispositioned for scrap for sterility failure investigation that was inadvertently shipped to customers.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution.Official notice →
  9. 2023-08-16
  10. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls Total Hip Kit, REF DYNJ903275S; surgical convenience kit

    The prep solution included in the Total Hip Kit expires prior to the expiration date of the Kit.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the state of Illinois.Official notice →
  11. 2023-08-09
  12. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. A V FISTULA,…

    Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldWorldwide distribution - US Nationwide and the countries of Canada, China,…Official notice →
All 117 MEDLINE INDUSTRIES, LP - Northfield recalls →

Other drugs & medical recalls in the United States

  1. 2023-09-27
  2. US
    Drugs & medicalClass II

    Philips North America Llc recalls Patient Information Center iX with Software Version Number 4.x in the following: (1) Patient Information Center iX Product Number:…

    Patient Information Center (PIC iX) Release 4.x Surveillance Crash Caused by Intel Graphics Driver Error-with a blank screen and subsequently require a manual reboot of the hardware to restart and continue central…

    FDA · DevicePhilips North America LlcNationwide Foreign: Austria Bahrain Belgium Canada Czech Republic Denmark…Official notice →
  3. US
    Drugs & medicalClass II

    Encore Medical, LP recalls DJO Surgical: Empowr Knee, Universal Tibia Baseplate, 6R, REF: 352-02-106

    Orthopedic device components were not subjected to final sterilization before shipment, which if implanted may lead to varying degrees of infection, which may require treatment, prolonged monitoring, and may lead to…

    FDA · DeviceEncore Medical, LPUS: AL, AZ, CA, CO, FL, IL, IN, KS, KY, LA, MA, MI, MN, MO, NC, NJ, NY, OH,…Official notice →
  4. US
    Drugs & medicalClass II

    Stryker Corporation recalls Stryker ACM (Advanced Cement Mixing) System: ACM Kit w/ Femoral Breakaway Nozzle-Allows the user to mix bone cement witha constant high…

    Potential for the Break-Away Femoral Nozzle the applicator tip connecting the cement cartridge, to disassemble or break off during use, can lead to the potential for loss of function of the ACM system and…

    FDA · DeviceStryker CorporationNationwide Foreign: Austria Belgium Canada France Germany Hong Kong Italy…Official notice →
  5. US
    Drugs & medicalClass II

    Aquila Corporation recalls APK2 Pressure-Sensing Wheelchair Cushions

    Defective battery pack in wheelchair cushions can overheat resulting in property damage and one possible injury.

    FDA · DeviceAquila CorporationWorldwide distribution: US (nationwide) and OUS (foreign) countries of:…Official notice →
  6. US
    Drugs & medicalClass II

    SenTec AG recalls Membrane Changer Single-Use, REF MC, each package contains 3 changers; Membrane Changer Reloadable, REF MC-R, each package contains 3…

    During rework of components during the manufacturing process, an additional piece of material may have been left in the device, which may result in an impact on measurement performance.

    FDA · DeviceSenTec AGUS Nationwide distribution.Official notice →
  7. US
    Drugs & medicalClass II

    ARROW INTERNATIONAL Inc. recalls Arrow ErgoPack Pressure Injectable One-Lumen PICC, REF CDC-05541-HPK1A; catheter, intravascular

    This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.

    FDA · DeviceARROW INTERNATIONAL Inc.US Nationwide distribution.Official notice →
See all drugs & medical recalls →