FlexTip Plus Combined Spinal Epidural Catheterization recall
FlexTip Plus Combined Spinal Epidural Catheterization Kit, Product Code ASK-05500-BID
Why was FlexTip Plus Combined Spinal Epidural Catheterization 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: 23F19E0337 23F19J0065 23F19K0100 23F19L0218 23F19H0048 23F19J0314 23F19K0303 23F19M0007
- Product
- FlexTip Plus Combined Spinal Epidural Catheterization Kit, Product Code ASK-05500-BID
- 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)