ACS IR - Angio Pack recall
ACS IR - Angio Pack
Why was ACS IR - Angio Pack recalled?
Product was sterilized with a higher than specification EO concentration.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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?
Model JEIR37H, Lot 657211 UDI: 00191072151612
- Product
- ACS IR - Angio Pack
- Recalling firm
- American Contract Systems, Inc.
- Quantity
- 24 packs
- Distribution
- US Nationwide distribution in the states of IL, MO, NE, and TX.
- Recall date
- May 18, 2022
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)