FlexTip Plus Combined Spinal Epidural Catheterization recall
FlexTip Plus Combined Spinal Epidural Catheterization Kit, Product Code ASK-05560-TG1
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: 23F19A0154 23F19C0273 23F19F0029 23F19G0360 23F19M0226
- Product
- FlexTip Plus Combined Spinal Epidural Catheterization Kit, Product Code ASK-05560-TG1
- 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)