Devices

KimberlyClark Single Shot Epidural Pain Management Trays

Model / Serial
Lot numbers: 181024, 181129 181217, 181221, 181231, 182022, 182058, 182101, 182108, 182131, 182222, 182223, 182263, 182265, 182289, 182293, 182301, 182315, 181A074, 181A94, 181A154, 181A177, 181A286, 181A289, 181A369, 182A002, 182A005, 182A012, 182A055, 182A056, 182A057, 182A064, 182A074, 182A075/182A78, 182A085, 182090, 182A142, 182AA144, 182A151, 182A155, 182A178, 182A194, 182A196, 182A198, 182A202, 182A204, 182A212, 182A216 and 189A001 (syringe).
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
U.S. Nationwide Distribution
Product Description
Kimberly-Clark Single Shot Epidural Pain Management Trays containing the BD LOR Syringe (BD Code 405198) || Product Usage: || The device is designed to provide regional anesthesia. The device may contain syringes, needles and drugs
Manufacturer
Kimberly-Clark Corporation
1 Event
- Recall of KimberlyClark Single Shot Epidural Pain Management Trays

Manufacturer

Kimberly-Clark Corporation

Manufacturer Address
Kimberly-Clark Corporation, 1400 Holcomb Bridge Rd, Roswell GA 30076-2190
Manufacturer Parent Company (2017)
Kimberly-Clark Corporation
Source
USFDA

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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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