MEDLINE STERILE IRIS SCISSORS CVD/STD REF DYNJ04049 (case)… recallZ-2024-2024 · MEDLINE INDUSTRIES, LP - Northfield · initiated Apr 30, 2024
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 - Northfield 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 the potential of the tip protector to fall off 4.5" sterile, curved, Iris Scissors
FDA root cause category: Under Investigation by firm
What the company is doing
Medline Industries, LP issued a recall notice to its consignees on 04/30/2024 via email and USPS First Class Mail. The notice explained the issued, potential risk, and requested the product be destroyed. Those who further distributed the affected product were directed to notify those to whom the affected product was distributed.
Recall details
- Recall number
- Z-2024-2024
- Status
- Open, Classified
- Initiated by the company
- Apr 30, 2024
- Posted by the FDA
- Jun 6, 2024
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Quantity
- 67811 units
- Product code
- JOK
- Distribution
- Worldwide distribution - US Nationwide and the countries of Singapore, Canada.
Product description
MEDLINE STERILE IRIS SCISSORS CVD/STD REF DYNJ04049 (case) and DYNJ04049H (individual unit)
Code information (models, lots, serial numbers)
UDI/DI 10080196847273, Lot Numbers: 23GBV681, 23HBD138, 23IBF254, 23LBJ787
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- MEDLINE DYNJ04049Medline Industries, Inc. · SCISSORS, GENERAL, SURGICAL3 recalls2 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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