Epidural Catheterization KIT recall
EPIDURAL CATHETERIZATION KIT, Product Code FR-05501-12
Why was Epidural Catheterization KIT 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: 71F19A0623 71F19C1042 71F19E1144 71F19G2853 71F19K0248 71F19A2996 71F19C2596 71F19E2950 71F19H2549 71F19K2117 71F19B1149 71F19D2545 71F19G1138 71F19J1815 71F19L0436
- Product
- EPIDURAL CATHETERIZATION KIT, Product Code FR-05501-12
- 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)