Sterile Radiology Procedure Kits, Model Number DYNDH1491B recallZ-1693-2026 · Medline Industries, LP · initiated Feb 18, 2026
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Medline Industries, LP or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility.
FDA root cause category: Under Investigation by firm
What the company is doing
An URGENT MEDICAL DEVICE RECALL notification letter dated 2/18/26 was sent to customers. REQUIRED ACTION: 1. Immediately check your stock for the affected item number(s) and the affected lot number(s) listed within the recall portal. Quarantine all affected product. Upon completion of the below actions, please destroy affected product. 2. Please use the link and the information below to complete your response form. Please list the quantity of affected product you have in inventory on the form. Even if you do not have any affected product in inventory, please complete and submit the response form. Website link: https://recalls.medline.com Recall Reference #: R-26-015-FG Recall Code: 3. Your account will receive credit once the response form is submitted. 4. If you are a distributor, or have resold or transferred this product to another company or individual, you are required by FDA regulations to notify them of this recall communication. Please request that customers destroy any affected product. You should include your customers quantities on your response form. If you have any questions, contact the Recall Department at 866-359-1704 or [email protected].
Recall details
- Recall number
- Z-1693-2026
- Status
- Open, Classified
- Initiated by the company
- Feb 18, 2026
- Posted by the FDA
- Mar 27, 2026
- Recalling firm
- Medline Industries, LP
- Quantity
- 420 units
- Product code
- LRO
- Distribution
- US Nationwide distribution in the state of MN.
Product description
Sterile Radiology Procedure Kits, Model Number DYNDH1491B
Code information (models, lots, serial numbers)
UDI-DI: (CS) 40198459071455, (EA) 10198459071454; Lot Number: 25GBB924
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- Medline Industries, Inc. DYNDH1491BMedline Industries, Inc. · General surgery tray1 recall0 reports
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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