Recall Z-0361-2016
Quest Medical, Inc. · initiated October 28, 2015
Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature
Product
Model 5001102 MPS Delivery Set w/ arrest agent and additive cassettes, heat exchanger &10 ft. delivery tubing; Model 5001102-AS MPS Delivery Set with 6 ft. delivery tubing; Model 7001102 MPS Low Volume Delivery Set for use with cardiopulmonary bypass equipment.
Codes / lots: 0491795E04, 0492175E04, 0492185E06, 0492195E06, 0492615E06, 0492625E08, 0492635E08, 0489905Y04, 0490245Y06, 0493075U02, 0493085U02, 0493435U04, 0493675U04, 0493685U07, 494465U07, 0494475U09, 0494855G01, 0495215U11, 0495225U11, 0495505G02, 495515G02, 0496535G08, 0496875G08, 496885G08, 0497245S02, 0495205U11, 497255S04, 0497655S04, 0498535S06, 0498545S06, 0492205E03, 0493695U04, 0494485U07, 0495525G02, 0497265S02, 0495965G04, 0492765E07
Reason for recall
The products have been found to intermittently exhibit a seal failure during use.
FDA-determined cause: Equipment maintenance
Action taken
The recalling firm issued a press release on 10/28/2015. The press release was posted on FDA website on 10/29/2015. The recalling firm emailed affected consignees on 10/28/15 and sent out recall letters via USPS beginning 10/30/15.
Details
- Recall number
- Z-0361-2016
- Initiated
- October 28, 2015
- Posted by FDA
- December 2, 2015
- Terminated
- November 17, 2016
- Product code
- DTR – Heat-Exchanger, Cardiopulmonary Bypass
- Quantity
- 18,761 units
- Distribution
- Distributed US (nationwide) and the countries of Canada, Japan, Saudi Arabia, Kuwait, South Africa, Switzerland, France, and Italy.
- Recalling firm
- Quest Medical, Inc., Allen, TX