Data Foundry

Medical device recalls 2016

Stryker PowerPRO — Class II medical device recall Z-1990-2016

Terminated recall by Stryker Medical Division of Stryker Corporation, reported 2016-06-22, distributed nationwide. Complaints of smoke coming from the foot end of the cot. This reportedly occurred when either the battery wa

Recall numberZ-1990-2016
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmStryker Medical Division of Stryker Corporation, Portage, MI, United States
Recall initiated2016-05-05
Classified2016-06-14
Reported by FDA2016-06-22
Terminated2017-09-18
DistributedNationwide (US)
Countries outside the USAU, CA, CH, ES, GB, HK
Quantity770
Serial numbers150740131, 150740132, 150740133, 150740134, 150740135, 150740136, 150740137, 150740138, 150740289, 150740290, 150740291, 150740292, 150740293, 150740294, 150740295, 150740296, 150740297, 150740298, 150740299, 150740550, 150740551, 150740552, 150740553, 150740554, 150740555 and 475 more
Model numbers6506-000-000, 6516-000-000, 6550-000-000

Product

Stryker PowerPRO (XT, IT, or TL) Cots Stretcher, Wheeled The Stryker Power-PRO" are powered ambulance cots are designed to support and transport a maximum weight of 700 lb. (318 kg) in pre-hospital and hospital environments.

Reason for recall

Complaints of smoke coming from the foot end of the cot. This reportedly occurred when either the battery was placed into the cot or shortly after placing the battery into the cot. In addition to the alleged smoking, one of the reports had also noted that when the user attempted to lower the cot (prior to the alleged smoking) the device went into high speed retract and then a few moments later i

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-1990-2016. 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.