Description/REF: EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05502-VM1 — Class I medical device recall Z-2371-2026
Ongoing recall by ARROW INTERNATIONAL, LLC, reported 2026-06-24, distributed nationwide. Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits an
| Recall number | Z-2371-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | ARROW INTERNATIONAL, LLC, Morrisville, NC, United States |
| Recall initiated | 2026-04-21 |
| Classified | 2026-06-12 |
| Reported by FDA | 2026-06-24 |
| Distributed | Nationwide (US) |
| Quantity | 1,525,831 |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 10801902140644, 10801902193275, 10801902202090, 10801902202144, 10801902202199, 10801902202250, 10801902202496, 10801902209501, 10801902209518, 10801902209525, 10801902209532, 10801902209549, 10801902209556, 10801902209570, 10801902209617, 10801902209631, 10801902209662, 10801902209716, 10801902209723, 10801902209730, 10801902209747, 10801902209754, 10801902209761, 10801902209785, 10801902209853 and 25 more |
| Lot numbers | 10801902140644/33F25J0944, 10801902193275/33F24C0256, 10801902193275/33F24D0103, 10801902193275/33F24E0156, 10801902193275/33F24G0485, 10801902193275/33F24G0561, 10801902202090/33F24E0580, 10801902202199/33F24D0154, 10801902202250/33F24B0319, 10801902202496/33F24C0049, 10801902209518/33F24E0057, 10801902209525/33F24C0015, 10801902209532/33F24G0331, 10801902209549/33F24C0019, 10801902209549/33F24J0277, 10801902209631/33F24D0153, 10801902209662/33F24J0603, 10801902209723/33F24L0572, 10801902209730/33F24E0497, 10801902209754/33F25C0165, 10801902209860/33F24J0617, 10801902209938/33F25C0168, 10801902209952/33F24E0514, 10801902209969/33F24L0643, 10801902209976/33F24D0389, 10801902209983/33F24G0483, 10801902210002/33F24K0550, 10801902210057/33F24J0628, 10801902210217/33F24D0038, 10801902210217/33F24D0380, 10801902210217/33F24D0382, 10801902210217/33F24D0385, 10801902210217/33F24K0246, 10801902210224/33F24J0657, 10801902210361/33F24D0418, 10801902210392/33F24K0235, 10801902211221/33F25G0137, 10801902211405/33F24E0516, 10801902214857/33F24E0505, 30801902121722/33F24J0501 and 460 more |
| Model numbers | 10801902140644/33F25J0944, 10801902193275/33F24C0256, 10801902193275/33F24D0103, 10801902193275/33F24E0156, 10801902193275/33F24G0485, 10801902193275/33F24G0561, 10801902202090/33F24E0580, 10801902202199/33F24D0154, 10801902202250/33F24B0319, 10801902202496/33F24C0049, 10801902209501, 10801902209518/33F24E0057, 10801902209525/33F24C0015, 10801902209532/33F24G0331, 10801902209549/33F24C0019, 10801902209549/33F24J0277, 10801902209556, 10801902209631/33F24D0153, 10801902209662/33F24J0603, 10801902209716, 10801902209723/33F24L0572, 10801902209730/33F24E0497, 10801902209747, 10801902209754/33F25C0165, 10801902209860/33F24J0617 and 475 more |
Product
Description/REF: EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05502-VM1; EPIDURAL CATHETERIZATION KIT: 19 GA/AK-05501; EPIDURAL CATHETERIZATION KIT/AK-05502; EPIDURAL CATHETERIZATION KIT/AK-05502D; EPIDURAL CATHETERIZATION KIT/AK-05503; EPIDURAL CATHETERIZATION KIT/AK-05503-L; SPINAL ANES/EPIDURAL CATH KIT/AK-05560; SPINAL ANES/EPIDURAL CATH KIT/ASK-02520-SBMC1; EPIDURAL CATHETERIZATION KIT/ASK-05400-BW1; EPIDURAL CATHETERIZATION KIT/ASK-05400-GH; SPINAL ANES/EPIDURAL CATH KIT/ASK-05401-LMC; EPIDURAL CATHETERIZATION KIT/ASK-05401-NM; SPINAL ANES/EPIDURAL CATH KIT/ASK-05500-BID1; EPIDURAL CATHETERIZATION KIT: 19 GA/ASK-05500-JHH1; EPIDURAL CATHETERIZATION KIT: 19 GA/ASK-05500-MCV1; EPIDURAL CATHETER KIT: 19GA X 90CM ASK-05500-MVH; EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05500-UMC; 19 GA X 35.5 IN EPIDURAL CATHETER KIT/ASK-05502-MLH; SPINAL ANES/EPIDURAL CATH KIT/ASK-05560-JMH1; SPINAL ANES/EPIDURAL CATH KIT/ASK-05560-MKD2; SPINAL ANES/EPIDURAL CATH KIT/ASK-05560-OM1; EPIDURAL CATHETERIZATION KIT/ASK-17019-SM; EPIDURAL CATHETERIZATION KIT/BP-05501; EPIDURAL CATHETERIZATION KIT/CK-05401; EPIDURAL CATHETERIZATION KIT/HS-05501; EPIDURAL CATHETERIZATION KIT/MM-05501; EPIDURAL CATHETERIZATION KIT: 19 GA/MP-17019-TK; EPIDURAL CATHETERIZATION KIT: 19 GA/MP-17019-TKD; EPIDURAL CATHETERIZATION KIT: 19 GA/MP-17019-TKL; EPIDURAL CATHETERIZATION KIT/MSO-05401-JMH; EPIDURAL CATHETERIZATION KIT/NM-05401; EPIDURAL CATHETERIZATION KIT/SJ-05501; EPIDURAL CATHETERIZATION KIT/SM-05401; EPIDURAL CATHETER KIT: 19 GA X 90 CM/TM-05401; EPIDURAL CATHETERIZATION KIT/TM-05502; SPINAL ANES/EPIDURAL CATH KIT/UI-05502; SPINAL ANES/EPIDURAL CATH KIT: 19 GA/ASK-05400-SHM; EPIDURAL CATH KIT: 19 GA/ASK-05400-UOM; EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05500-MR; EPIDURAL CATHETERIZATION KIT: 19 GA/ASK-05500-TM; EPIDURAL CATHETERIZATION KIT/ASK-05501-BHL1; EPIDURAL CATHETERIZATION KIT/ASK-05501-GH; EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05501-SM; EPIDURAL CATHETERIZATION KIT/ASK-05502-BSM; EPIDURAL CATHETERIZATION KIT/ASK-05502-MGH1; EPIDURAL CATHETERIZATION KIT/ASK-05503-BWB1; EPIDURAL CATHETERIZATION KIT/ASK-05503-HMH; EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05503-SPH; EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05503-UPM1; SPINAL ANES/EPIDURAL CATH KIT/ASK-05560-UCI2; EPIDURAL CATHETERIZATION KIT: 19 GA/ASK-17019-UMP; EPIDURAL CATHETERIZATION KIT/MH-05503-1; EPIDURAL CATHETERIZATION KIT/ASK-05401-VB2; Epidural Catheterization Kit: 19GA/ASK-05500-SC1; Epidural Catheterization Kit: 19GA/ASK-05500-SC3; EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05501-AFH1; EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05501-BMC; EPIDURAL CATHETERIZATION KIT/ASK-05502-NY; EPIDURAL CATHETERIZATION KIT/ASK-17019-RMH
Reason for recall
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2371-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.