RecallRadar

FDA Device recall Z-1782-2014

Cooper Surgical TAMPA CATHETER 5 French 33 cm

On 2014-06-18 the FDA classified a Class II recall of Cooper Surgical TAMPA CATHETER 5 French 33 cm by Coopersurgical, citing sterility of the device may be compromised due to unsealed pouch.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1782-2014
ClassificationClass II
Statusterminated
Initiated2014-05-13
Published2014-06-18
Last updated2026-09-13 11:53 UTC
CompanyCoopersurgical
DistributionUS

Product

Cooper Surgical TAMPA CATHETER 5 French 33 cm. Intended for Hysterosonography. Model Number: 61-2005

Reason

Sterility of the device may be compromised due to unsealed pouch

Identifiers

code_infoLot 141525

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1782-2014%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.