International Medical Devices Database

Manufacturer Address
Handicare USA, Inc., 2201 Hangar Pl, Ste 200, Allentown PA 18109-9342
Manufacturer Parent Company (2017)
Handicare Group Ab
Source
USFDA
2 Events
- Recall of ReTurn 7400/7500
- Recall of Device Recall Re Turn

2 devices in the database

ReTurn 7400/7500

Model / Serial
Model # 7400, 7500 and 7322 (spare part) Serial # 373317697270501334, 373317697270501430, 073317697400500012, 073317697400500057
Product Classification
Physical Medicine Devices
Device Class
1
Implanted device?
No
Distribution
US Distribution to the states of : NY, NJ, NV, NE, IL, CT, PA and ME
Product Description
ReTurn 7500/7500 || Aid, transfer

Device Recall Re Turn

Model / Serial
All affected product in the U.S are from the same LOT #1402S, Model #s 6133-6136
Product Classification
Physical Medicine Devices
Device Class
1
Implanted device?
No
Distribution
US Distribution to the states of : FL, CA, NJ, NC and MD.
Product Description
ReTurn belt, wipeable, sizes Small through Extra Large, Plastic pouch, 1 item per pouch. Patient transfer aid.

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Disclaimer

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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Handicare USA, Inc.

2 devices in the database

ReTurn 7400/7500

Device Recall Re Turn