Teleflex Medical: Medical Device Recall in 2017 - (Recall #: Z-2251-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Hudson RCI, Pediatric Nasal Cannula, Non-Flared Prongs, Rx only,

Product Classification:

Class II

Date Initiated: May 9, 2017

Date Posted: June 14, 2017

Recall Number: Z-2251-2017

Event ID: 77230

Reason for Recall:

Incorrect labeling; the box label indicates Pediatric, the product insert indicates an Adult device.

Status: Terminated

Product Quantity: 1150 units

Code Information:

Product Code: 1101, Lot numbers: 74J1603122, 74K1601506, 74K1602306 and 74L16006.

Distribution Pattern:

CA, CT, FL, IL, IN, MD, MI, MN, MO, MS, NC, NJ, NY, NV, OH, PA, TX, VA, WI and WV.

Voluntary or Mandated:

Voluntary: Firm initiated