FlexTip Plus Epidural Catheterization Set recall
FlexTip Plus Epidural Catheterization Set, Product Code AA-05400-E
Why was FlexTip Plus Epidural Catheterization Set recalled?
There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
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?
Lots: 71F19B2081 71F19C1655 71F19E2128 71F19G2444 71F19B2586 71F19E1245 71F19F1432 71F19J1685
- Product
- FlexTip Plus Epidural Catheterization Set, Product Code AA-05400-E
- Recalling firm
- Arrow International Inc
- Quantity
- 343,105 total
- Distribution
- The products were distributed to the following US states: AK, AR, AZ, CA, CO, CT, FL, GA, ID, IL, IN, LA, MA, MD, MI, MN, MO, MT, NC, NE, NH, NJ, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, and WY.
- Recall date
- February 19, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)