Stryker Medical Division of Stryker Corporation: Stryker Power-PRO TL cot-powered ambulance cot Model Number 6550 - Product Usage: is a powered wheeled stretcher that is intended to support and transport the entire body of a traumatized, ambulatory or non-ambulatory human patient (includes infants and adults).

Recall number

Z-1935-2020

Recalling firm

Stryker Medical Division of Stryker Corporation

Product

Stryker Power-PRO TL cot-powered ambulance cot Model Number 6550 - Product Usage: is a powered wheeled stretcher that is intended to support and transport the entire body of a traumatized, ambulatory or non-ambulatory human patient (includes infants and adults).

Status

Terminated

Initiated

2020-04-07

Posted

not on file

Terminated

2021-01-22

Reason

Ambulance Cots may not meet crash test standard BS EN 1789

Root cause

Component change control

Action

Stryker issued Initial notification to International distribution partners via electronic notification system on 4/7/20. Customers will be notified by written letter distributed via traceable methods. Letter states reason for recall, health risk and action to take: 1. Locate the units listed on the attached business reply form and identify the address where they can be serviced. 2. Return the enclosed business reply form to confirm receipt of this notification by fax or email 269 488 8691 or email productfieldaction@stryker.com the enclosed acknowledgement of this notification. Power-PRO" TL cot crash test standard Model: 6550 GTIN: 07613327261660 Month dd, yyyy Attn: Recall Coordinator/ Fleet Manager URGENT: URGENT: MEDICAL DEVICE MEDICAL DEVICE MEDICAL DEVICE MEDICAL DEVICE CORRECTIONCORRECTIONCORRECTION CORRECTION CORRECTIONCORRECTION Model numbers Product description Serial number(s) 6550-000-000 Power-PRO" TL cot manufactured between Sept 9, 2019 and Nov 7, 2019 See Attachment Pg. 2 3. Upon receipt of the completed business reply form, Stryker will contact you to arrange for the modification/repair of your Power-PRO " TL cot. 4. If you have loaned or sold any of the products listed in this letter, please forward a copy of this notice to the new users and advise us of their new location in the space provided on the business reply form. 5. If you have disposed of any of these units and they are no longer in use, please, advise us of their obsolescence by providing us with their serial number in the space provided on the business reply form. If you have any questions or concerns, please contact Customer Service +1 800 327 0770. Our normal business hours are Monday-Friday 8 a.m-6 p.m. (EST).

Quantity

34 units

Distribution

Foreign: UK

Lot, serial or model codes

Serial Numbers: 1909003700051  1909003700052  1909003700055  1909003700056  1909003700057  1909003700058  1909003700059  1909003700060  1909003700061  1909003700062  1909003700065  1909003700066  1909003700067  1909003700068  1909003700069  1909003700070  1909003700072  1909003700073  1909003700074  1909003700075  1909003700076  1909003700077  1909003700078  1909003700079  1909003700080  1909003700081  1909003700082  1909003700083  1909003700084  1909003700085  1909003700086  1909003700087  1909003700088  1909003700090

510(k) numbers

not on file

PMA numbers

not on file

Product code

INK

Firm FEI

1831750

Firm city

Portage

Firm state

MI

Firm country

not on file

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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