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Stryker Medical Division of Stryker Corporation Recall 91716

Description: Power-PRO 2 . Intended as an ambulance cot to transport a patient to or from an emergency or non-emergency location. Model: 650705550001

Stryker Medical Division of Stryker Corporation Recall 91716 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-1256-2023
Event ID91716
Event DescriptionPower-PRO 2 . Intended as an ambulance cot to transport a patient to or from an emergency or non-emergency location. Model: 650705550001
Product TypeDevices
DistributionUS Nationwide distribution in the states of NY, VA.
Quantity4 units
Recall ReasonTransport Cot has insufficient volume of epoxy to assemblies installed in the head section and foot sectioning system may result in separation of head end or foot end from the cot and result in unexpected disengagement while loading/unloading or transport.
Device Classification20230322
Device Code InfoGTIN: 07613327559118 Serial Numbers: 2208002066, 2208002071, 2209001508, 2208001664
Center Classification Date20230315
Recall Initiation Date20230201
Recalling FirmStryker Medical Division of Stryker Corporation
Initial Notification Letter
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