FDA Device recall Z-1990-2016

Stryker PowerPRO (XT, IT, or TL) Cots Stretcher, Wheeled The Stryker Power-PRO" are powered ambulance cots are designed to support and tran…

FDA Device
Class II
terminated
Published 2016-06-22

On 2016-06-22 the FDA classified a Class II recall of Stryker PowerPRO (XT, IT, or TL) Cots Stretcher, Wheeled The Stryker Power-PRO" are powered ambulance cots are designed to support and tran… by Stryker Medical Division, citing 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 c….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-1990-2016
Classification	Class II
Status	terminated
Initiated	2016-05-05
Published	2016-06-22
Last updated	2026-09-13 11:54 UTC
Company	Stryker Medical Division
Distribution	US

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

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

Identifiers

code_info	Model numbers: 6506-000-000, 6516-000-000, 6550-000-000 Serial Numbers 150740131 150740132 150740133 1507401… Model numbers: 6506-000-000, 6516-000-000, 6550-000-000 Serial Numbers 150740131 150740132 150740133 150740134 150740135 150740136 150740137 150740138 150740289 150740290 150740291 150740292 150740293 150740294 150740295 150740296 150740297 150740298 150740299 150740550 150740551 150740552 150740553 150740554 150740555 150740556 150740557 150740558 150740559 150740560 150740561 150740562 150740563 150740564 150740565 150740566 150740567 150740568 150740569 150740570 150740587 150740588 150740589 150740590 150740591 150740592 150839490 150840425 150840426 150840427 150840428 150840429 150840430 150840431 150840432 150840433 150840434 150840435 150840436 150840437 150840438 150840439 150840440 150840441 150840442 150840443 150840444 150840445 150840446 150840447 150840448 150840449 150840450 150840493 150840495 150840496 150840497 150840498 150840499 150840550 150840551 150840552 150840553 15084055

code_info

Model numbers: 6506-000-000, 6516-000-000, 6550-000-000 Serial Numbers 150740131 150740132 150740133 1507401…

Model numbers: 6506-000-000, 6516-000-000, 6550-000-000 Serial Numbers 150740131 150740132 150740133 150740134 150740135 150740136 150740137 150740138 150740289 150740290 150740291 150740292 150740293 150740294 150740295 150740296 150740297 150740298 150740299 150740550 150740551 150740552 150740553 150740554 150740555 150740556 150740557 150740558 150740559 150740560 150740561 150740562 150740563 150740564 150740565 150740566 150740567 150740568 150740569 150740570 150740587 150740588 150740589 150740590 150740591 150740592 150839490 150840425 150840426 150840427 150840428 150840429 150840430 150840431 150840432 150840433 150840434 150840435 150840436 150840437 150840438 150840439 150840440 150840441 150840442 150840443 150840444 150840445 150840446 150840447 150840448 150840449 150840450 150840493 150840495 150840496 150840497 150840498 150840499 150840550 150840551 150840552 150840553 15084055

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1990-2016%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.