Basin SET recall: Labeling Error
BASIN SET, MEBS42K, general surgical kit
Why was Basin SET recalled?
Basin Set labeling error: components within the kit are for the Single Basin Set. Therefore, the contents of the package do not match the contents listed on the label.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI/DI 00191072151742, Batch/Lot No. 833221, exp 6/16/2023
- Product
- BASIN SET, MEBS42K, general surgical kit
- Recalling firm
- American Contract Systems, Inc.
- Quantity
- 1504 trays
- Distribution
- US Nationwide distribution.
- Recall date
- November 30, 2022
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)