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.…

Read the official notice →
Date
2026-04-01
Country
United States
Brand
Medline Industries
Product
Puracol and Puracol Plus Collagen Wound Dressings: MSC8522 DRESSING,COLLAGEN,PURACOL,STRL,2" X 2" MSC8622EP DRESSING,COLLAGEN,PURACOL…
Classification
Class II
Units
Domestic distribution nationwide US. International distribution to Mexico and…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 THORACIC ROBOTS, DYNJ908777B

    Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with…

    FDA · DeviceMedline Industries, LPUS Nationwide distribution in the states of CA, FL, IL, IN, KY, MA, MD, MT,…Official notice →
  3. 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 →
  4. 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 →
  5. 2026-03-18
  6. US
    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…

    FDA · DeviceMedline Industries, LPDomestic distribution nationwide US. International distribution to Panama,…Official notice →
  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 →
All 75 Medline Industries recalls →

Other drugs & medical recalls in the United States

  1. 2026-04-08
  2. US
  3. US
    Drugs & medicalClass II

    Amneal Pharmaceuticals, LLC recalls traMADol Hydrochloride Tablets, USP, 50 mg, 500-count bottles, Rx only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Ahmedabad…

    Failed Impurities/Degradation Specifications: N-nitroso-desmethyl-tramadol impurity (NDSRI) was found out of the specification at 24-month stability interval during Long term stability (25¿C/60%RH).

    FDA · DrugAmneal Pharmaceuticals, LLCNationwide within the USAOfficial notice →
  4. 2026-04-01
  5. US
    Drugs & medicalClass II

    Waldemar Link GmbH & Co. KG (Mfg Site) recalls Embrace Drill Tower, Wedged (25mm); Item Number: 645-081/62;

    The surgical technique for the Embrace Shoulder Instruments - Drill Tower has mixed-up article numbers in the overview of the instruments. However, the individual surgical steps described in the surgical technique are…

    FDA · DeviceWaldemar Link GmbH & Co. KG (Mfg Site)US distribution to states of: AL, AZ, FL, GA, IL, IN, KS, KY, LA, MI, NC, OH,…Official notice →
  6. US
    Drugs & medicalClass II

    CareFusion 303, Inc. recalls BD Alaris" System with Guardrails" Suite MX with Point of Care Unit

    Due to product labeling not indicating which Transport Layer Security (TLS) version that must be enabled on hospital network to ensure secure Wi-Fi communication with Point-of-Care Units

    FDA · DeviceCareFusion 303, Inc.Worldwide distribution: U.S.(Nationwide) to states of: AL, AR, AZ, CA, CO, CT,…Official notice →
  7. US
    Drugs & medicalClass II

    Olympus Corporation of the Americas recalls Brand Name: Olympus PKS Cutting Forceps, 5mm 33cm Product Name: PKS Cutting Forceps Model/Catalog Number: 3005PK Product…

    Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting Forceps' jaw breaking during clinical use.

    FDA · DeviceOlympus Corporation of the AmericasWorldwide - US Nationwide and the countries of Canada, Mexico, EU, Australia,…Official notice →
  8. US
    Drugs & medicalClass II

    Tandem Diabetes Care, Inc. recalls Tandem pumps are battery-operated infusion pumps capable of both basal and bolus delivery of insulin. The pumps utilize a motor-driven…

    The Czech language user guide contained multiple translation errors. The most significant error was that it incorrectly instructs users to verify that the infusion set is connected to the body, when it should instead…

    FDA · DeviceTandem Diabetes Care, Inc.International distribution in the countries of Czech Republic, Slovakia.Official notice →
See all drugs & medical recalls →