PLUS 30 PRIORITY PACK Accessory Kit Product Usage: Is recall
PLUS 30 PRIORITY PACK Accessory Kit Product Usage: Is recommended for use during vascular procedures in conjunction with interventional and / or…
Why was PLUS 30 PRIORITY PACK Accessory Kit Product Usage: Is recalled?
Incorrect expiration being entered for one lot.
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?
Device Identifier #: 08717648 01360 7 Part Number: 1000185 Lot number: 60047593
- Product
- PLUS 30 PRIORITY PACK Accessory Kit Product Usage: Is recommended for use during vascular procedures in conjunction with interventional and / or…
- Recalling firm
- Abbott Vascular
- Quantity
- 26 units
- Distribution
- US Nationwide Distribution - NC and NY
- Recall date
- March 6, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)