Data Foundry

Medical device recalls 2020

10 cc Luer-Slip Loss of Resistance Syringe — Class II medical device recall Z-1205-2020

Terminated recall by Arrow International Inc, reported 2020-02-19, distributed in AK, AR, AZ, CA, CO, CT, FL, GA…. There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits re

Recall numberZ-1205-2020
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmArrow International Inc, Reading, PA, United States
Recall initiated2020-01-15
Classified2020-02-13
Reported by FDA2020-02-19
Terminated2023-03-17
DistributedAK, 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, WY
Quantity343,105 total
Lot numbers13F18J0916, 13F18K0675, 13F18L0737, 13F18M0178, 13F19C0321, 13F19D0335, 13F19E0141, 13F19E0212, 13F19G0070, 13F19G0071, 13F19G0458, 13F19H0085, 13F19H0274, 13F19H0275, 13F19H0634, 13F19J0038, 13F19J0039, 13F19J0040, 13F19J0596, 13F19K0097, 13F19L0252

Product

10 cc Luer-Slip Loss of Resistance Syringe, Product Code LR-05501

Reason for recall

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.

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-1205-2020. 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.