PACK GENERAL ROBOTIC. Medical convenience kit recall
PACK GENERAL ROBOTIC. Medical convenience kit.
Why was PACK GENERAL ROBOTIC. Medical convenience kit recalled?
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
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 No. RDLD047-10; UDI: 10809160358603; Kit Lot No. 1589630, 1590570, 1610157, 1617028, 1618142, 1621537, 1629589, 1635288, 1636852.
- Product
- PACK GENERAL ROBOTIC. Medical convenience kit.
- Recalling firm
- AVID Medical, Inc.
- Quantity
- 656 units
- Distribution
- Domestic: CA, IL, MD, OH, PA, TX, WA.
- Recall date
- August 13, 2025
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)