Multi-Track Angiographic Catheter recall
Multi-Track Angiographic Catheter (MMTA) Product Code: MMTA05100 Product Usage: Recommended for use in catheterization for angiography of…
Why was Multi-Track Angiographic Catheter recalled?
Instructions for Use booklets were not included on the outer pouch
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?
Lot numbers: 5MT-1264, 5MT-1265 Exp. Date: 2023-09-30 UDI: 04046964312700
- Product
- Multi-Track Angiographic Catheter (MMTA) Product Code: MMTA05100 Product Usage: Recommended for use in catheterization for angiography of…
- Recalling firm
- Numed Inc
- Quantity
- 100 units
- Distribution
- US distribution in the state of PA
- Recall date
- December 5, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)