Devices

Device Recall Stryker Renaissance Series Stretchers

Model / Serial
Model 1231: 39 Units 0310049178, 0310049179, 0311058120, 0312050809, 0407059532, 0407059533, 0407059656, 0407059657, 0407059851, 0407059852, 0407059853, 0407059854, 0407059855, 0407059856, 0407059857, 0407059858, 0407059859, 0407059860, 0407059861, 0407059862, 0407059863, 0407059864, 0407059865, 0407059866, 0407059867, 0407059868, 0407059869, 0407059870, 0408059073, 0408059123, 0408059124, 0408059871, 0408059872, 0408059873, 0408059874, 0408059875, 0408059876, 0408059877, and 0409062555.
Product Classification
Physical Medicine Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution -- USA, Canada, Brazil, Japan, Singapore, Spain, and the Far East.
Product Description
Stryker Renaissance Series Stretchers, Model 1231Z Emergency Care with Zoom, Stryker Medical, Portage, MI.
Manufacturer
Stryker Medical Div. of Stryker Corporation
1 Event
- Recall of Device Recall Stryker Renaissance Series Stretchers

Manufacturer

Stryker Medical Div. of Stryker Corporation

Manufacturer Address
Stryker Medical Div. of Stryker Corporation, 3800 E. Centre Ave., Portage MI 49002
Source
USFDA

One device with a similar name

Learn more about the data here

Device Recall Stryker Renaissance Series Stretchers

Model / Serial
Model 1731: 19 Units 0306055261, 0306055262, 0311054605, 0311054606, 0311058060, 0311058130, 0311058491, 0311058492, 0312050810, 0406059715, 0406059835, 0406059836, 0406059837, 0407059289, 0407059290, 0407059291, 0409062599, 0409064150, and 0409064258.
Product Classification
Physical Medicine Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution -- USA, Canada, Brazil, Japan, Singapore, Spain, and the Far East.
Product Description
Stryker Renaissance Series Stretchers, Model 1731Z PACU with Zoom, Stryker Medical, Portage, MI.
Manufacturer
Stryker Medical Div. of Stryker Corporation

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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