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.
Read the official notice →- Date
- 2026-10-21
- Country
- United States
- Brand
- Medline Industries
- Product
- Medline surgical convenience kits labeled as: 1) OPEN HEART PACK A & B, Medline Product number/SKU DYNJ04584L; 2) OPEN HEART ACCESSORY…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- 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
- 2026-10-28
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.
FDA · DeviceMedline Industries, LPWorldwide distribution - US Nationwide and the countries of CA, TC, AU, AE.Official notice →- 2026-10-21
Medline Industries, LP recalls Medline convenience kit labeled as: FOOT ANKLE. Medline Kit SKU DYNJ65395A
Discrepancy in the shelf-life of a component
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 →- 2026-10-14
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 →- 2026-10-07
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 →- 2026-09-30
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…
USOther drugs & medical recalls in the United States
- 2026-10-21
Merit Medical Systems, Inc. recalls Scout MD, REF MDS05A-01, MDS05C-01, MDS10C-01 Contents: (1) Scout MD Delivery System, Standard for use with the SCOUT MD Surgical…
The implantable clip may experience difficulties deploying, which could prevent the reflector from functioning as intended during use.
INTELERAD MEDICAL SYSTEMS INCORPORATED recalls IntelePACS, InteleConnect Portal/Tech Portal Versions PACS-5-1-1-R102, PACS-5-2-1-R93, PACS-5-3-1-R83 through R128,…
Following a Chromium-based web-browser, report and displayed images may not match.
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 →Howmedica Osteonics Corp. recalls TS Universal Baseplate Finishing Tray, Triathlon. Catalog Number: 6543-6-506.
Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the 30-minute dry time may lead to a small amount of residual…
FDA · DeviceHowmedica Osteonics Corp.These trays are provided by sale or loan. Loans are provided through…Official notice →Cook Incorporated recalls Williams Cystoscopic Injection Needles, used for cystoscopic injection into the urethra, bladder neck, and bladder wall, Reference Part…
The female Luer lock adapter component in the affected device lots may not have been correctly seated due to misalignment and inadequate torquing during manufacturing. Potential events that may occur as a result of…
FDA · DeviceCook IncorporatedUS States: FL, IL, NM, TX, WA. Canada, France, Germany, Italy, Spain,…Official notice →Magellan Diagnostics, Inc. recalls LeadCare II Blood Lead Test Kit. Model/Catalog Number: 70-6762.
In kit sub-lot 2530M-01 the date of expiration printed on the outer labeling may indicate the wrong expiration date of July 22, 2026 while the correct expiration date is July 13, 2026. If used the system will display…
FDA · DeviceMagellan Diagnostics, Inc.US Nationwide distribution in the states of CA, IN, PA, TX, NE, IL, MA, MO, KY.Official notice →