Argon Medical Devices, Inc: Medical Device Recall in 2015 - (Recall #: Z-2189-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

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

Product Classification:

Class II

Date Initiated: June 18, 2015

Date Posted: July 29, 2015

Recall Number: Z-2189-2015

Event ID: 71533

Reason for Recall:

Potential defect in the forming of the primary package of the blister that may compromise the sterility of the product inside the tray.

Status: Terminated

Product Quantity: 10290 units

Code Information:

Lot Numbers: 11088295, 11088596, 11088597, 11089105, 11089366, 11094182, 11094681, 11094912, 11095381, 11095844, 11095845, 11095951, 11096558, 11097278, 11097504, 11098024, 11098647, 11099173

Distribution Pattern:

Voluntary or Mandated:

Voluntary: Firm initiated