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).
FDA Recall Z-1935-2020 · Posted None
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Recalling FirmStryker Medical Division of Stryker Corporation
Recall StatusTerminated
Product CodeINK
Date Initiated2020-04-07
Date Terminated2021-01-22
Product Quantity34 units
Reason for Recall
Ambulance Cots may not meet crash test standard BS EN 1789
Firm 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 [email protected] 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).
Root Cause
Component change control
Distribution Pattern
Foreign: UK
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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