PowerGlide ST Midline Catheter Maximal Barrier Kit-18 recall
PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge,10 cm length Catalog Number: ST018101D
Why was PowerGlide ST Midline Catheter Maximal Barrier Kit-18 recalled?
Iincorrectly packaged without the required lidocaine as labeled
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 Number: REDW0476 20 Exp. Date: 20OCT30 UDI: (01)00801741139390
- Product
- PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge,10 cm length Catalog Number: ST018101D
- Recalling firm
- Becton Dickinson & Company
- Quantity
- 655 kits
- Distribution
- AZ, CT, GA, IL, LA, MA, MI, MN, ND, NE, NY, OH, SD, TX),
- Recall date
- May 20, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)