RegWardenFDA facility compliance records
Recall

Class III — Hardy Diagnostics

Recalling firmHARDY DIAGNOSTICS
Registered facilityView this company's 2 registered facilities → (openFDA recall records do not name a specific facility)
ClassificationClass III
StatusTerminated
ReasonStreptococcus culture medium contains an incorrect expiration date. The culture medium outer box labeling contains an expiration date of 2021-11-10 instead of the correct expiration date of 2020-11-10
ProductStrep B Carrot Broth One-Step, Ref. Z40, UDI: 00819398026499
Quantity8,620 units
DistributionUS: VA, AR, WI, ID, NY, AL, CA, MT, TX, MN, NH, WA, NC, NY, AZ, AK, MO, FL, MI, WY, ID, CO, AL, MT, WY, Puerto Rico, and Guam
Initiated2020-10-06
Classified2020-11-09
Terminated2021-05-28
Recall numberZ-0441-2021
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 III recall — Hardy Diagnostics (Z-0441-2021).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/86586/

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