Data Foundry

Medical device recalls 2021

HAMILTON HEATER SHAKER — Class II medical device recall Z-1156-2021

Ongoing recall by Hamilton Co, reported 2021-03-10, distributed in AL, AR, AZ, CA, CO, CT, DC, DE…. There is a risk that the device can start a fire if flammable liquids contact and enter the device.

Recall numberZ-1156-2021
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmHamilton Co, Reno, NV, United States
Recall initiated2021-01-15
Classified2021-02-27
Reported by FDA2021-03-10
DistributedAL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WY
Countries outside the USAT, AU, BR, CA, CH, CL, CN, CO, DE, FI, GB, IT, JP, KR, PE, PY, RO, SG, TH, UY
Quantity4,729 units
Model numbers19903400, 199034R, 3MM, HHS2

Product

HAMILTON HEATER SHAKER, 115 VAC/ 230 VAC, 750 VA, Power Consumption 41V/ 100W (max.), Relative Humidity 15% - 85% no condensation. REF 19903400

Reason for recall

There is a risk that the device can start a fire if flammable liquids contact and enter the device.

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-1156-2021. 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.