Medline Iris Scissors, Single-Use, Curved, Standard 4.5… recallZ-0465-2025 · MEDLINE INDUSTRIES, LP - Northfield · initiated Oct 21, 2024
Class II Open, Classified All recalls posted in November 2024
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
Tip protector may fall off within the packaging, resulting in compromised sterile barrier system and loss of sterility.
FDA root cause category: Under Investigation by firm
What the company is doing
This is an expansion of recall RES 92881, which was originally initiated on April 30, 2024. Additional impacted customers were identified and notified on October 7, 2024. Customers were instructed to destroy any affected product on hand. The firm will issue credit for affected product.
Recall details
- Recall number
- Z-0465-2025
- Recall class
- Class II
- Status
- Open, Classified
- Initiated by the company
- Oct 21, 2024
- Posted by the FDA
- Nov 14, 2024
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Quantity
- 69,611
- Product code
- LRW
- Distribution
- US Nationwide distributions in the states of AL, AR, CO, CT, FL, IA, IN, KS, LA, MA, MO, NC, NY, OK, OR, RI, TN, TX, VA, WA, WY.
Product description
Medline Iris Scissors, Single-Use, Curved, Standard 4.5 , Model Nos. DYNJ04049 (cases), DYNJ04049H (eaches)
Code information (models, lots, serial numbers)
UDI-DI: 10080196847273 Lots 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 18, 2026. Text above is shown as published by the FDA.
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