FDA Enforcement Class II Terminated

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

Recall: Z-1205-2020 · Reported February 19, 2020

Enforcement

Recall Number
Z-1205-2020
Event ID
84726
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Arrow International Inc
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
February 19, 2020
Initiation Date
January 15, 2020
Classification Date
February 13, 2020
Termination Date
March 17, 2023
Address
2400 Bernville Rd, Reading, PA, 19605-9607, United States

Description

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

Reason

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.

Code Info

Lots: 13F18J0916 13F19C0321 13F19G0070 13F19H0274 13F19J0039 13F19L0252 13F18K0675 13F19D0335 13F19G0071 13F19H0275 13F19J0040 13F18L0737 13F19E0141 13F19G0458 13F19H0634 13F19J0596 13F18M0178 13F19E0212 13F19H0085 13F19J0038 13F19K0097

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.

Quantity

343,105 total