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Wealy® RELI®

MYCO MEDICAL SUPPLIES INC. · Model SS3ML21G101 · UDI-DI 00386120009155

MEG Prescription
1
510(k) clearances
2,941
Adverse events
17
Recalls
138
Facilities

Description

Safety Syringe w/ Ndl, 3ML, 21G x 1"

Recalls

DateFirmReason
2024-09-25Cardinal Health 200, LLCCertain lots of listed lots of Cardinal Health Monoject U-100 1 mL Insulin Syringe Luer-Lock with Tip Cap Soft Pack have demonstrated incompatibility with needleless Intravenous (I
2022-06-10Guangdong Haiou Medical Apparatus Co., LtdComplaints received in which needle and needle holder have detached from the syringe after injection as well as needle not retracting into the syringe as per intended use, resultin
2022-06-10Guangdong Haiou Medical Apparatus Co., LtdComplaints received in which needle and needle holder have detached from the syringe after injection as well as needle not retracting into the syringe as per intended use, resultin
2021-05-17Smiths Medical ASD Inc.Specific models and lot numbers of the Jelco Hypodermic Needle-Pro Fixed Needle Insulin Syringe 29Gx1/2 odd number line graduation markings on the syringe barrel were skewed approx
2015-11-23Terumo Medical CorpPotential improper bonding between the tube and luer for certain lots of Surflo Winged Infusion Set with Filter and Needle Protection (Surshield).
2013-07-10Smiths Medical ASD, Inc.Visible orange/ brown particulate on the needles of the 29g Hypodermic Needle-Pro Fixed Needle Insulin Syringes
2013-07-10Smiths Medical ASD, Inc.Visible orange/ brown particulate on the needles of the 29g Hypodermic Needle-Pro Fixed Needle Insulin Syringes
2013-07-10Smiths Medical ASD, Inc.Visible orange/ brown particulate on the needles of the 29g Hypodermic Needle-Pro Fixed Needle Insulin Syringes
2013-07-10Smiths Medical ASD, Inc.Visible orange/ brown particulate on the needles of the 29g Hypodermic Needle-Pro Fixed Needle Insulin Syringes
2013-07-10Smiths Medical ASD, Inc.Visible orange/ brown particulate on the needles of the 29g Hypodermic Needle-Pro Fixed Needle Insulin Syringes

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.