Repro-Med Systems, Inc.: Medical Device Recall in 2019 - (Recall #: Z-0051-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

20" 2-Needle 26-Gauge 6mm HlgH-Flo Subcutaneous Safety Needle Sets" Product # RMS22606 - Product Usage: RMS HlgH-Flo Subcutaneous Safety Needle Sets are intended for the delivery of medication to the subcutaneous tissue.

Product Classification:

Class II

Date Initiated: August 20, 2019

Date Posted: October 16, 2019

Recall Number: Z-0051-2020

Event ID: 83650

Reason for Recall:

Mislabeled needle lengths

Status: Terminated

Product Quantity: 1990 pouches

Code Information:

Lot # N.78648 GTIN: 00659443000292

Distribution Pattern:

US Nationwide distribution including the states of NJ, OH, FL, GA, IL, MA, CA, TX, NC, IA, NV, OR, MD, TN, VA, NY.

Voluntary or Mandated:

Voluntary: Firm initiated