Drugs & medicalClass II

Medline Industries, LP recalls MEDLINE convenience kits labeled as: 1) ACH PLASTICS BREAST-LF, REF CDS983639K; 2) BREAST ABD, REF CDS984267J; 3) PLASTIC PACK, REF…

Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing SafeAir Smoke Evacuation Pencils. Stryker Instruments has expanded the scope of their recall of SafeAir Smoke…

Read the official notice →
Date
2025-11-26
Country
United States
Brand
Medline Industries
Product
MEDLINE convenience kits labeled as: 1) ACH PLASTICS BREAST-LF, REF CDS983639K; 2) BREAST ABD, REF CDS984267J; 3) PLASTIC PACK, REF…
Classification
Class II
Units
US Nationwide distribution.
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 Details may be shortened or out of date; the official notice is the authoritative source.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 recalls

  1. 2025-12-17
  2. US
    Drugs & medicalClass II

    Medline Industries, LP recalls DEXLOCK Achilles Repair Implant Kits, MAKT4520

    There have been multiple complaints of drill bit fusing to the bushing/sleeve within the drill guide during use. Retrieving a replacement drill bit and drill guide may prolong the surgical procedure.

    FDA · DeviceMedline Industries, LPUS Nationwide distribution in the states of AL, AR, AZ, CO, DE, FL, GA, ID,…Official notice →
  3. US
    Drugs & medicalClass II

    Medline Industries, LP recalls Quick Strip Fabric Sterile Adhesive Bandages, 1" x 3", Medline Item Number NON25660QS

    Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.

    FDA · DeviceMedline Industries, LPUS, Guam, Canada, United Arab EmiratesOfficial notice →
  4. US
    Drugs & medicalClass II

    Medline Industries, LP recalls MEDLINE PERFUSION SYRINGE, REF: DYNJ39223C

    Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing BD Luer Tip Caps. BD has issued a recall of their Luer Tip Caps after confirming through internal testing that…

    FDA · DeviceMedline Industries, LPUS Nationwide distribution in the state of CA.Official notice →
  5. 2025-11-26
  6. US
    Drugs & medicalClass II

    Medline Industries, LP recalls MEDLINE STERILE BASIC EYE PACK 16: 1) REF: DYNJ37743D; 2) REF: DYNJ37743F.

    Medline has identified specific sterile eye procedure kits with pouch packaging that may exhibit open seals.

    FDA · DeviceMedline Industries, LPUS: MOOfficial notice →
  7. 2025-11-19
  8. US
    Drugs & medicalClass II

    Medline Industries, LP recalls Medline Renewal LigaSure Blunt Tip Sealer/Divider, Compatible with FT10 Generator, 5 mm x 37 cm FT10 SW Version 4.0.1.15 or lower;…

    Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged.

    FDA · DeviceMedline Industries, LPUS Nationwide distribution.Official notice →
  9. US
    Drugs & medicalClass I

    Medline Industries, LP recalls Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; OPEN HEART SUPPLEMENT DYNJ909116D; VASCULAR DYNJ909124F

    Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to hypoxia, hypoventilation, and inadequate delivery of inhaled anesthetic…

    FDA · DeviceMedline Industries, LPInternational distribution to Mexico and Panama. US nationwide distribution to…Official notice →
All 75 Medline Industries recalls →

Other drugs & medical recalls in the United States

  1. 2025-11-26
  2. US
    Drugs & medicalClass II

    Exactech, Inc. recalls Brand Name: Equinoxe Ergo Product Name: Adjustable Angle rTSA Reamer, 46mm Model/Catalog Number: 321-59-46 Software Version: N/A Product…

    Due to products that have not completed design updates and performance testing being released/distributed. Products may not conform to design and performance criteria.

    FDA · DeviceExactech, Inc.U.S.: SC O.U.S.: N/AOfficial notice →
  3. US
    Drugs & medicalClass II

    Quest International, Inc. recalls Brand Name: ReQuest Measles IgG Product Name: Rubeola IgG Enzyme Linked Immunoabsorbant Assay Model/Catalog Number: 01-190 Software…

    Due to distributing the measles IgG IVD without a premarket approved/cleared.

    FDA · DeviceQuest International, Inc.All products were distributed in the United States. (Utah, Washington).Official notice →
  4. US
    Drugs & medicalClass II

    Merit Medical Systems, Inc. recalls PhD Hemostasis Valve, REF: IN4802/K, IN4802/T, IN4918/A, IN7802/C, IN8802/C, IN9802, IN9802/A, K05-02166B, K05T-02138A, K12T-10798A,…

    Hemostasis valve has a manufacturing defect and when used the valve cap may remain depressed, leading to potential leakage, which may result in procedure inconvenience and/or hemorrhage.

    FDA · DeviceMerit Medical Systems, Inc.US: PA, AZ, LA, CO, FL, NC, SC, OH, AK, IL, IA, MN, TX, WI, AR, NY, CA, KS,…Official notice →
  5. US
    Drugs & medicalClass II

    Medline Industries, LP recalls MEDLINE STERILE BASIC EYE PACK 16: 1) REF: DYNJ37743D; 2) REF: DYNJ37743F.

    Medline has identified specific sterile eye procedure kits with pouch packaging that may exhibit open seals.

    FDA · DeviceMedline Industries, LPUS: MOOfficial notice →
  6. US
    Drugs & medicalClass II

    Medtronic Perfusion Systems recalls MC3 VitalFlow Console, REF 58100; Blood pump of ecmo

    As of August 6, 2025, Medtronic has received eleven reports of VitalFlow Consoles displaying an E70 error code during normal operation. When this occurs, the touch screen may become temporarily unresponsive and go…

    FDA · DeviceMedtronic Perfusion SystemsUS Nationwide distribution.Official notice →
  7. US
    Drugs & medicalClass II

    Thoratec LLC recalls Brand Name: HeartMate Product Name: HeartMate 3 Controller (Standalone) Model/Catalog Number: 106531US, HeartMate 3 Controller, US;…

    Due to potential corrosion issues associated with the Backup Battery cable connector that may cause a Backup Battery Fault Alarm.

    FDA · DeviceThoratec LLCWorldwide - US Nationwide distribution including in the states of AK, AL, AR,…Official notice →
See all drugs & medical recalls →