Arrow International Recalls Epidural Catheterization Kits Due to Syringe Failure Risk
Arrow International is recalling 343,105 epidural catheterization kits because the included loss of resistance syringes may fail, potentially causing dural puncture.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class II and involves a medical device defect that results in dural puncture, a significant injury requiring medical intervention (blood patch), which aligns with the 'Severe' criteria for significant injury reports.
Plain-English summary
Arrow International Inc is recalling 343,105 units of the Epidural Catheterization Kit (Product Code BE-05400B-ETTEL). The recall involves specific lots: 71F19C0509, 71F19G0116, 71F19H1409, 71F19J1840, 71F19D2945, 71F19G2238, and 71F19J0078.
The recall was initiated because there is a potential for various failures with the loss of resistance (LOR) syringes included in the kits. These failures can result in dural puncture, with some instances requiring a blood patch for treatment.
The affected 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. Healthcare providers and facilities should check their inventory for the listed lot numbers and stop using the affected kits.
The recalled product
- Product
- EPIDURAL CATHETERIZATION KIT, Product Code BE-05400B-ETTEL
- Manufacturer
- Arrow International Inc
- Affected units
- 343,105
Distribution
Part of a larger recall action
This product is one of 49 recalled by Arrow International Inc under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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