Repro-Med Systems recalls
Repro-Med Systems has 3 recalls on record with the FDA and USDA, the earliest in 2018 and the latest reported on 16 Oct 2019. The most frequent reason is sterility.
Total recalls3since 2018
Last 12 months0reported
Class I00% of total
Ongoing0latest 16 Oct 2019
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 3 100%Class III 0 0%
Why repro-med systems is recalled
Product types
By year
All repro-med systems recalls, newest first
3 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | 20" 2-Needle 26-Gauge HlgH-Flo Subcutaneous Safety Needle recalled | Repro-Med Systems | Labeling Errors | Nationwide |
| Device | CLASS II | HIgH-Flo Subcutaneous Safety Needle Sets, 2-Needle Set/ Needles recalled | Repro-Med Systems | Sterility | Nationwide |
| Device | CLASS II | Freedom60 Precision Flow Rate Tubing Sets recalled by Repro-Med Systems | Repro-Med Systems | Sterility | Nationwide |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.