Marketing brochures for the PowerPICC and PowerPICC recall
Marketing brochures for the PowerPICC and PowerPICC SOLO catheters
Why was Marketing brochures for the PowerPICC and PowerPICC recalled?
Bard Access Systems is recalling marketing brochures for the PowerPICC¿ and PowerPICC¿ SOLO¿ catheters due to incorrect indication for use contained in the brochure.
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?
The brochures were purchased from the vendor on 04/14/2015, Code S120667R0
- Product
- Marketing brochures for the PowerPICC and PowerPICC SOLO catheters
- Recalling firm
- Bard Access Systems
- Quantity
- 1811
- Distribution
- Distributed to domestic and foreign conference attendees.
- Recall date
- September 30, 2015
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)