Codman & Shurtleff, Inc.: Medical Device Recall in 2015 - (Recall #: Z-1684-2015)

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:

CODMAN 3000 Series Refill Set- Huber needles. Used in combination with the CODMAN 3000 Series Constant Flow Implantable Pump CATALOG NO. : AP-07014 Each CODMAN 3000 Refill Kit contains 2 (two) 22 Gauge x 1.5 Huber Point Needles which are used in conjunction with a 50 mL Calibrated Syringe Barrel, Tubing Set and Stopcock for pump refills. .

Product Classification:

Class II

Date Initiated: March 5, 2015

Date Posted: June 3, 2015

Recall Number: Z-1684-2015

Event ID: 70659

Reason for Recall:

Needle is leaking from hub/needle cannula connection

Status: Terminated

Product Quantity: 5463 units

Code Information:

Lot numbers: 14B114CT, 14E011CT, and 14E366CT

Distribution Pattern:

Worldwide Distribution-US (nationwide) and the countries of Canada, France, Germany, and Switzerland.

Voluntary or Mandated:

Voluntary: Firm initiated