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Devices
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
1 Event
Recall of Device Recall Bone Marrow Biopsy Needle
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Manufacturer
Argon Medical Devices, Inc
Manufacturer Address
Argon Medical Devices, Inc, 1445 Flat Creek Rd, Athens TX 75751-5002
Manufacturer Parent Company (2017)
RoundTable Healthcare Partners Lp
Source
USFDA
One device with a similar name
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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.
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