RegWardenFDA facility compliance records
Recall

Class II — MHC Medical Products LLC

Recalling firmMHC Medical Products, LLC
Registered facilityMHC Medical Products (the firm's only registered facility)
ClassificationClass II
StatusOngoing
ReasonThe retail shelf cartons may be labeled with an incorrect lot number.
ProductEasyTouch (ET) Insulin Syringe 29G 1ml " (Item 829155) Product Usage: INTENDED FOR INJECTION OF U100 INSULIN ONLY
Quantity3137 retail units (313700 syringes)
DistributionUS Nationwide Distribution in the states of: AR, AZ, CA, FL, GA, IL, IN, LA, MA, MI, MO, MS, NC, ND, NH, NJ, NV, NY, OH, PA, SC, TN, TX, VA, WA, WI, WV, and Puerto Rico.
Initiated2018-04-06
Classified2018-05-09
Recall numberZ-1779-2018
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — MHC Medical Products LLC (Z-1779-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/79950/

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