Data Foundry

Medical device recalls 2019

LW Scientific ZIP IQ Combo Centrifuge — Class II medical device recall Z-1049-2019

Terminated recall by LW Scientific, Inc., reported 2019-04-03, distributed nationwide. The clear, plastic, polycarbonate hematocrit rotor may break apart during use and be ejected through the plast

Recall numberZ-1049-2019
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmLW Scientific, Inc., Lawrenceville, GA, United States
Recall initiated2019-02-06
Classified2019-03-22
Reported by FDA2019-04-03
Terminated2021-05-07
DistributedNationwide (US)
Countries outside the USAU, CA, GT, HN, NI, NZ, PE, PH, SG, SV, TT
Quantity226 units
Reason classesdevice malfunction
Serial numbers6C1712002, 6C1712008, 6C1803021, 6C1803022, 6C1803053, 6C1803054, 6C1803055, 6C1803057, 6C1803058, 6C1803059, 6C1803060, 6C1803097, 6C1803124, 6C1803128, 6C1803129, 6C1803134, 6C1803135, 6C1803136, 6C1803140, 6C1805146, 6C1805147, 6C1805148, 6C1805149, 6C1805150, 6C1805151 and 198 more

Product

LW Scientific ZIP IQ Combo Centrifuge, ZIC-CMBO-2RT3 Rev B Product Usage: used as a general purpose centrifuge to spin down blood in hematocrit tubes with additional rotor to spin other fluids in test tubes (15ml)

Reason for recall

The clear, plastic, polycarbonate hematocrit rotor may break apart during use and be ejected through the plastic housing, posing a safety hazard to the technician and potentially damaging the surrounding area.

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-1049-2019. 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.