FlexTip Plus Epidural Catheterization Set recall
FlexTip Plus Epidural Catheterization Set, Product Code MP-17019-TIP
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: 13F19A0544 13F19B0451 13F19E0017 13F19K0394 13F19A0796 13F19D0481 13F19G0086 13F19L0070
- Product
- FlexTip Plus Epidural Catheterization Set, Product Code MP-17019-TIP
- 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)