Drugs & medicalClass II

Medline Industries, LP recalls Medline Medcrest Surgical Gowns: MDTGXC4J5XL DBQ-GOWN,SURG,XALT,L4, CRTCL CVR, GRN, 5 MDTGXC4JL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,L…

Fabric may experience premature delamination when using included laundering instructions. Identifying delaminated gown or drape in a surgical setting may result in brief delay in patient care. If delaminated product is…

Read the official notice →
Date
2026-03-18
Country
United States
Brand
Medline Industries
Product
Medline Medcrest Surgical Gowns: MDTGXC4J5XL DBQ-GOWN,SURG,XALT,L4, CRTCL CVR, GRN, 5 MDTGXC4JL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,L…
Classification
Class II
Units
Domestic distribution nationwide US. International distribution to Panama,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2026-04-08
  2. US
    Drugs & medicalClass II

    Medline Industries, LP recalls Sterile Radiology Procedure Kits, Model Number DYNDH1491B

    There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility.

    FDA · DeviceMedline Industries, LPUS Nationwide distribution in the state of MN.Official notice →
  3. US
    Drugs & medicalClass II

    Medline Industries, LP recalls Medline Kits containing ENFIT G-TUBE CONNECTOR 1. SKU DYKM2720 G/J TUBE CARE KIT 2. SKU ENFITDISCKIT ENFIT DISCHARGE KIT

    Connectors were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices, which could lead to leakage. Leakage may result in delayed care and fluid loss.…

    FDA · DeviceMedline Industries, LPWorldwide - US Nationwide and the countries of Canada.Official notice →
  4. 2026-04-01
  5. US
    Drugs & medicalClass II

    Medline Industries, LP recalls Puracol and Puracol Plus Collagen Wound Dressings: MSC8522 DRESSING,COLLAGEN,PURACOL,STRL,2" X 2" MSC8622EP DRESSING,COLLAGEN,PURACOL…

    Elevated endotoxin levels identified in affected lots. Issue may elicit strong inflammatory response if used, including local tissue irritation, delayed wound healing, or systemic effects such as fever and hypotension.…

    FDA · DeviceMedline Industries, LPDomestic distribution nationwide US. International distribution to Mexico and…Official notice →
  6. 2026-03-18
  7. US
    Drugs & medicalClass II

    Medline Industries, LP recalls Medline Kits containing Cardinal Health s Aqua-Seal Chest Drainage Unit: 1) OPEN HEART, Model Number: DYNJ902487A; 2) CARDIAC PROCEDURE,…

    The instructions for use (IFUs) on specified Cardinal Health Chest Drainage Units (CDUs) and accessories have been updated to clarify the intended target patient population as adults, 18 years and older.

    FDA · DeviceMedline Industries, LPWorldwide - US Nationwide distribution in the state of CA and the countries of…Official notice →
  8. 2026-03-04
  9. US
    Drugs & medicalClass II

    Medline Industries, LP recalls Medline Kits containing Tego Connectors Medline DIALYSIS ON/OFF KIT SKU EBSI1746

    Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an occluded fluid path identified…

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

    Medline Industries, LP recalls Medline Convenience Kits: 1) NAIL KIT, Model Number: DYKM1528

    Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.

    FDA · DeviceMedline Industries, LPWorldwide distribution - US Nationwide and the countries of Bahamas, Bermuda,…Official notice →
All 75 Medline Industries recalls →

Other drugs & medical recalls in the United States

  1. 2026-03-25
  2. US
    Drugs & medicalClass III

    Annora Pharma Private Limited recalls Pitavastatin Tablets, 2 mg, packaged in 90-count bottles, Rx only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141,…

    Presence of foreign tablets/capsules: one Pitavastatin tablet 1mg found in bottle of Pitavastatin tablets 2mg

    FDA · DrugAnnora Pharma Private LimitedTNOfficial notice →
  3. US
    Drugs & medicalClass II

    STRIDES PHARMA INC recalls Children's Ibuprofen Oral Suspension, USP, 100 mg per 5mL, 4 FL OZ (120 mL) bottle, Manufactured for: Taro Pharmaceuticals U.S.A., Inc.,…

    Presence of foreign substance: the firm received complaints for a gel-like mass and black particles in the product.

    FDA · DrugSTRIDES PHARMA INCU.S.A. NationwideOfficial notice →
  4. 2026-03-19
  5. US
    Drugs & medical

    Infant Walkers Recalled Due to Risk of Serious Injury or Death from Fall Hazard; Violate Mandatory Standard for Infant Walkers; Sold on Amazon by Goregent Official Store

    The recalled infant walkers violate the mandatory standard for infant walkers because they can fit through a standard doorway and fail to stop at the edge of a step, posing a risk of serious injury or death due to a…

  6. 2026-03-18
  7. US
    Drugs & medicalClass II

    Medline Industries, LP recalls Medline Kits containing Cardinal Health s Aqua-Seal Chest Drainage Unit: 1) OPEN HEART, Model Number: DYNJ902487A; 2) CARDIAC PROCEDURE,…

    The instructions for use (IFUs) on specified Cardinal Health Chest Drainage Units (CDUs) and accessories have been updated to clarify the intended target patient population as adults, 18 years and older.

    FDA · DeviceMedline Industries, LPWorldwide - US Nationwide distribution in the state of CA and the countries of…Official notice →
  8. US
  9. US
    Drugs & medicalClass II

    Lutronic Corporation recalls CLARITY II Laser System; Model No. 1110200210.

    Reports of devices sparking/popping and potentially burning patients.

    FDA · DeviceLutronic CorporationWorldwide distribution - US Nationwide and the countries of Canada, South…Official notice →
See all drugs & medical recalls →