Data Foundry

Medical device recalls 2019

Stryker Heated Tube Set with Real-Time Pressure Sensing — Class II medical device recall Z-1728-2019

Terminated recall by Stryker Corporation, reported 2019-06-12, distributed nationwide. The heated tube sets were consistently leaking and detaching from the cassette.

Recall numberZ-1728-2019
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmStryker Corporation, San Jose, CA, United States
Recall initiated2019-03-07
Classified2019-06-04
Reported by FDA2019-06-12
Terminated2024-03-08
DistributedNationwide (US)
Countries outside the USAE, AR, BR, CA, CL, CO, IN, JP, MX, SA, UY
Quantity19,083 boxes
Reason classespackaging, device malfunction
UPC / GTIN / UDI-DI07613327055658
Lot numbers56004333, 56004335, 56004337, 56004342, 56004352, 56004375, 56004393, 56004419, 56004421, 56004423, 56004435, 56004445, 56004447, 56004465, 56004481, 56004485, 56004512, 56004520, 56004534, 56004541, 56004575, 56004577, 56004586, 56004597, 56004602, 56004626, 56004630, 56004643, 56004645, 56004649, 56004651, 56004710, 56004723, 56004725, 56004741, 56004752, 56004754, 56004757, 56004782, 56004786 and 151 more
Model numbers0620-040-690

Product

Stryker Heated Tube Set with Real-Time Pressure Sensing (RTP), REF 0620-040-690, an accessory to the PNEUMO SURE High Flow Insufflator, Disposable, Rx, Sterile.

Reason for recall

The heated tube sets were consistently leaking and detaching from the cassette.

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-1728-2019. 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.