Recall Atlas
Drugs & medicalClass II

Medline Industries, LP recalls MEDLINE medical convenience kits labeled as: 1) HIP SCOPE PACK, Medline Kit Number/SKU DYNJ64103C; 2) HIP SCOPE PACK, Medline Kit…

Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.

Read the official notice →
Date
2026-10-28
Country
United States
Brand
Medline Industries
Product
MEDLINE medical convenience kits labeled as: 1) HIP SCOPE PACK, Medline Kit Number/SKU DYNJ64103C; 2) HIP SCOPE PACK, Medline Kit…
Classification
Class II
Units
Worldwide distribution - US Nationwide and the countries of CA, TC, AU, AE.
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2026-10-21
  2. Drugs & medicalClass II

    Medline Industries, LP recalls Medline convenience kit labeled as: FOOT ANKLE. Medline Kit SKU DYNJ65395A

    Discrepancy in the shelf-life of a component

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

    Medline Industries, LP recalls Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911135A CHN GYN ONCOLOGY DYNJ906731M

    Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during use, which may result in delays or ending procedures.

    FDA · DeviceMedline Industries, LPUS Nationwide distribution in the states of AZ, CA, IN, MD, MO, NJ, OH, and WI.Official notice →
  4. Drugs & medicalClass II

    Medline Industries, LP recalls Medline surgical convenience kits labeled as: 1) OPEN HEART PACK A & B, Medline Product number/SKU DYNJ04584L; 2) OPEN HEART ACCESSORY…

    Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use.

    FDA · DeviceMedline Industries, LPUS Nationwide distribution.Official notice →
  5. 2026-10-14
  6. Drugs & medicalClass II

    Medline Industries, LP recalls Rollator, Bariatric, Basic Steel, Blue, mechanical walker with four legs and a metal frame intended for medical purposes to provide…

    The front fork stem bolt/wheel assembly may disconnect from the rollator frame tubing. If the front fork stem bolt/wheel assembly disconnects from the rollator frame tubing, the front wheels may become loose or detach…

    FDA · DeviceMedline Industries, LPWorldwide distribution - US Nationwide and the country of Canada.Official notice →
  7. 2026-10-07
  8. Drugs & medicalClass I

    Medline Industries, LP recalls Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED, MANUAL, MEDLITE

    Potential fire hazard involving the hand control pendant and associated wiring used with affected beds. Pendant or pendant wiring may overheat, potentially leading to smoking, sparking, melting, burning, or fire.…

    FDA · DeviceMedline Industries, LPDistribution US Nationwide including territories of Puerto Rico and Guam and…Official notice →
  9. 2026-09-30
  10. Drugs & medicalClass II

    Medline Industries, LP recalls Medline Convenience Kits: 1) ANTERIOR SPINE PACK, Catalog Number: DYNJT10197; 2) CRANIOTOMY #IMF 56646-LF, Catalog Number: DYNJVB91001; 3)…

    The kits contain neurological sponges with the potential for unexpected variability of endotoxin levels. Potentially elevated endotoxin levels may present health risks that could require medical intervention, such as…

    FDA · DeviceMedline Industries, LPUS Nationwide.Official notice →
All 79 Medline Industries recalls →

Other drugs & medical recalls in the United States

  1. 2026-10-28
  2. Drugs & medicalClass II

    AVID Medical, Inc. recalls Halyard ANTERIOR HIP PACK. Model/Catalog Number: SOAH30.

    A non-sterile component was piggybacked and incorrectly placed outside of the sterile barrier and not subjected to EO sterilization per kit specifications.

    FDA · DeviceAVID Medical, Inc.US Nationwide distributor in the state of Arizona.Official notice →
  3. Drugs & medicalClass II

    Solstice Corporation recalls Xact mole marker for mammography Model/Catalog Number: M15RM

    The radiopaque material may detach from the marker. In some cases, artifact was noted and attributed to the detached material.

    FDA · DeviceSolstice CorporationWorldwide - US Nationwide distribution in the states and territory of CA, FL,…Official notice →
  4. Drugs & medicalClass II

    Medtronic Neuromodulation recalls InterStim Percutaneous Extensions EXT 3560022 ISTM II PERC 3560022 EXT 3560030 ISTM MICRO PERC 3560030

    Wrong lead or percutaneous extension selected. Use of an incompatible lead or percutaneous extension will prevent the system from working as intended and may result in delay of surgery or need for surgical replacement…

    FDA · DeviceMedtronic NeuromodulationWorldwide distribution - US Nationwide and territory of Puerto Rico. The…Official notice →
  5. Drugs & medicalClass II

    Medtronic MiniMed, Inc. recalls Generic Name: MiniMed Go App Generic Name: MiniMed Go App Model/Catalog Number: MMT-8600 (iOS), MMT-8601 (Android) Software Version:…

    A software defect in which existing users who had previously configured and enabled the long-acting dose reminder feature in version 1.2.0 or earlier experienced failure of the long-acting dose reminder after updating…

    FDA · DeviceMedtronic MiniMed, Inc.Worldwide - U.S. Nationwide distribution in the states of AL, CA, CT, FL, LA,…Official notice →
  6. Drugs & medicalClass II

    restor3d Inc. recalls Generic Name: restor3d MTP Implant Generic Name: MTP Implant Model/Catalog Number: 1103-161620 Software Version: None Product Description:…

    Implants were found in the field with orange sterilzation indicators which means implants were not exposed to sterilization.

    FDA · Devicerestor3d Inc.U.S. Nationwide distribution in the states of FL, IL, NC, PA, SC, and TX.Official notice →
  7. Drugs & medicalClass II

    Boston Scientific Cork, Ltd. recalls Direxion Torqueable Microcatheter, NGMC/SINGLE/021/SWAN/1RO/105; Material Number: M001195290

    The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridges on nitinol sleeves due to laser…

    FDA · DeviceBoston Scientific Cork, Ltd.Worldwide distribution US Nationwide and territory of Puerto Rico. The…Official notice →
See all drugs & medical recalls →