Centurion Sterile Weitlaner Retractor, Reorder: 67315 recallZ-1765-2025 · MEDLINE INDUSTRIES, LP - Northfield · initiated Apr 9, 2025
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
Three is the potential for the retractors to puncture through the sterile packaging.
FDA root cause category: Under Investigation by firm
What the company is doing
Medline issued a MEDLINE DEVICE RECALL notice to its consignees on 04/09/2025, The notice explained the issue, potential risk, and requested the following: 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.comRecall Reference #: R-25-072Recall Code: 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-1765-2025
- Status
- Open, Classified
- Initiated by the company
- Apr 9, 2025
- Posted by the FDA
- May 15, 2025
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Quantity
- 2100 units
- Product code
- GAD
- Distribution
- US Nationwide distribution.
Product description
Centurion Sterile Weitlaner Retractor, Reorder: 67315
Code information (models, lots, serial numbers)
UDI/DI 10653160379867 (each) 00653160379860 (case), Lot Numbers: 2020092801, 2020100601, 2021022601, 2021032301, 2021042301, 2021060101, 2021062101, 2021090790, 2022021190, 2022032390, 2022040690, 2022061690, 2022072690, 2022091490, 2023020990, 2023100590, 2023120790, 2024012990, 2024022290, 2024040590, 2024070290, 2024080190, 2024092790, 2025011490.
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- Centurion 67315Centurion Medical Products Corporation · RETRACTOR1 recall0 reports
Other products in the same recall event
The FDA groups related products into one recall event (event 96732).
- Z-1766-2025 · Open, ClassifiedCenturion Sterile Weitlaner Retractor 3 x 4 Prong, Reorder: I68395
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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