Devices

Device Recall Bone Marrow Biopsy Needle

Model / Serial
Lot Number 81371NGF and 81081MRM.
Product Classification
Gastroenterology-Urology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide - FL, TX, WI, PA, MN, SC, NC, KY, TN, CA, AR, OR, NJ, and IA.
Product Description
Angiotech, Bone Marrow Biopsy Needle, Medical Device Technologies, Inc. The device is intended for use during Bone Marrow Biopsy.
Manufacturer
Medical Device Technologies, Inc.
1 Event
- Recall of Device Recall Bone Marrow Biopsy Needle

Manufacturer

Medical Device Technologies, Inc.

Manufacturer Address
Medical Device Technologies, Inc., 3600 Sw 47th Ave, Gainesville FL 32608-7555
Manufacturer Parent Company (2017)
RoundTable Healthcare Partners Lp
Source
USFDA

One device with a similar name

Learn more about the data here

Device Recall Bone Marrow Biopsy Needle

Model / Serial
Lot Numbers: 11088295, 11088596, 11088597, 11089105, 11089366, 11094182, 11094681, 11094912, 11095381, 11095844, 11095845, 11095951, 11096558, 11097278, 11097504, 11098024, 11098647, 11099173
Product Classification
Gastroenterology-Urology Devices
Device Class
2
Implanted device?
No
Distribution
US
Product Description
T-Lok Bone Marrow Biopsy Needle 8G x 4 Ext Can, Part Number DBMNJ0804TL; T-Lok Bone Marrow Biopsy Needle 11G x 4 Ext Can, Part Number DBMNJ1104TL; Bone Marrow Biopsy Needle 13G x 4, Part Number DBMNJ1304
Manufacturer
Argon Medical Devices, Inc

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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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