FDA Device recall Z-0329-2014

Olympus Endoscopic Flushing Pump, Model OPF-2. Facilitates washing of tissues to remove blood, feces and other organic matter during endosc…

FDA Device
Class II
terminated
Published 2013-11-27

On 2013-11-27 the FDA classified a Class II recall of Olympus Endoscopic Flushing Pump, Model OPF-2. Facilitates washing of tissues to remove blood, feces and other organic matter during endosc… by Olympus America, citing there is a possibility that the pump head was not shipped in the locked position. If the pump head is in an unlocked position this may, under certain circumstances, cause the pump….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0329-2014
Classification	Class II
Status	terminated
Initiated	2013-05-20
Published	2013-11-27
Last updated	2026-09-13 11:53 UTC
Company	Olympus America
Distribution	US

Product

Olympus Endoscopic Flushing Pump, Model OPF-2. Facilitates washing of tissues to remove blood, feces and other organic matter during endoscopic procedures.

Reason

There is a possibility that the pump head was not shipped in the locked position. If the pump head is in an unlocked position this may, under certain circumstances, cause the pump to stop and go into power stand-by mode.

Identifiers

code_info	Model OPF-2 with serial numbers: 21301567 21301799 21220870 21220876 21220878 21220869 21301569 21220788 21220… Model OPF-2 with serial numbers: 21301567 21301799 21220870 21220876 21220878 21220869 21301569 21220788 21220710 21220712 21220181 21220707 21301315 21301216 21301672 21301675 21301793 21301795 21301960 21303157 21303159 21303161 21303388 21303390 21303391 21301064 21221126 21301053 21301059 21301570 21301573 21301054 21220701 21301066 21301203 21301205 21301209 21301673 21220706 21301572 21301052 21301055 21301065 21301571 21220953 21302798 21302917 21302920 21302925 21303009 21303017 21301058 21301060 21301485 21301493 21301566 21301408 21301961 21301804 21221123 21301317 21301483 21301217 21301320 21301482 21301214 21220357 21301062 21220179 21220171 21220789 21301487 21301489 21303156 21220877 21301413 21220176 21220711 21302919 21301796 21301797 21301415 21301963 21220174 21220168 21220704 21301056 21220621 21301204 21301207 21301212 21301215 21301575 21301206 21301213 21301321 213013

code_info

Model OPF-2 with serial numbers: 21301567 21301799 21220870 21220876 21220878 21220869 21301569 21220788 21220…

Model OPF-2 with serial numbers: 21301567 21301799 21220870 21220876 21220878 21220869 21301569 21220788 21220710 21220712 21220181 21220707 21301315 21301216 21301672 21301675 21301793 21301795 21301960 21303157 21303159 21303161 21303388 21303390 21303391 21301064 21221126 21301053 21301059 21301570 21301573 21301054 21220701 21301066 21301203 21301205 21301209 21301673 21220706 21301572 21301052 21301055 21301065 21301571 21220953 21302798 21302917 21302920 21302925 21303009 21303017 21301058 21301060 21301485 21301493 21301566 21301408 21301961 21301804 21221123 21301317 21301483 21301217 21301320 21301482 21301214 21220357 21301062 21220179 21220171 21220789 21301487 21301489 21303156 21220877 21301413 21220176 21220711 21302919 21301796 21301797 21301415 21301963 21220174 21220168 21220704 21301056 21220621 21301204 21301207 21301212 21301215 21301575 21301206 21301213 21301321 213013

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-0329-2014%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.