Data Foundry

Medical device recalls 2013

Mesa Labs Smart-Read 10^5 EZ Test BI Test Pack — Class II medical device recall Z-1827-2013

Terminated recall by Steritec Products Mfc. Co., Inc., reported 2013-08-07, distributed nationwide. Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a product recall involving the EZTest

Recall numberZ-1827-2013
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmSteritec Products Mfc. Co., Inc., Englewood, CO, United States
Recall initiated2013-06-10
Classified2013-07-29
Reported by FDA2013-08-07
Terminated2013-12-19
DistributedNationwide (US)
Countries outside the USAR, AU, CA, CZ, IT, TR
Quantity5,000 units
Reason classeslabeling
Lot numbers130301

Product

Mesa Labs Smart-Read 10^5 EZ Test BI Test Pack, SteriTec Product Code PL 298/25, Distributor Product Code SRSP/25 The Smart-Read Biological Test Pack with Instant Readout Integrator: is designed specifically for biological testing of 3 or 4 minutes or longer at 1132 (27270 and 3 minutes at 11357275re-vacuum steam sterilizers.

Reason for recall

Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a product recall involving the EZTest Steam and Smart-Read Biological Indicators (BI) because the readout time is not in specification with the label claims.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1827-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.