RegWardenFDA facility compliance records
Recall

Class II — Mercedes Medical, Inc.

Recalling firmMERCEDES MEDICAL LLC
Registered facilityMERCEDES MEDICAL LLC (the firm's only registered facility)
ClassificationClass II
StatusTerminated
ReasonNo 510(k) clearance
ProductLingen SAMPLE Disposable Virus Sampling Kit pack, Item SAM ENI MTM-04, containing 2 tubes and 2 swabs/pack; and SAM ENI MTM04TUBE, containing 1 tube/pack.
QuantitySAM ENI MTM04 - 58 packs; and SAM ENI MTM04TUBE - 49 packs
DistributionWorldwide distribution - US Nationwide distribution including in the states of Alabama, Arizona, California, Colorado, District of Columbia, Florida, Georgia, Iowa, Idaho, Illinois, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Missouri, Montana, North Carolina, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Pennsylvania, Texas, Virginia…
Initiated2021-06-10
Classified2021-07-12
Terminated2023-08-14
Recall numberZ-2067-2021
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 — Mercedes Medical, Inc. (Z-2067-2021).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/88088/

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