RecallRadar

FDA Device recall Z-1686-2022

Sensation Plus 8Fr 50cc Intra-Aortic Balloon Catheter

On 2022-09-14 the FDA classified a Class II recall of Sensation Plus 8Fr 50cc Intra-Aortic Balloon Catheter by Datascope, citing certain lots containing undersized dilator.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1686-2022
ClassificationClass II
Statusongoing
Initiated2022-08-05
Published2022-09-14
Last updated2026-09-13 11:56 UTC
CompanyDatascope
Distributionn/a

Product

Sensation Plus 8Fr 50cc Intra-Aortic Balloon Catheter

Reason

Certain lots containing undersized dilator.

Identifiers

code_info
Code information reads "UDI-DI, Lot No., Finished Goods Part No.": 10607567108605, 3000168086, 0684-00-0576-01; 1060756…Code information reads "UDI-DI, Lot No., Finished Goods Part No.": 10607567108605, 3000168086, 0684-00-0576-01; 10607567108605, 3000217952, 0684-00-0576-01; 10607567109633, 3000166607, 0684-00-0576-01U; 10607567109633, 3000169722, 0684-00-0576-01U; 10607567109633, 3000172352, 0684-00-0576-01U; 10607567109633, 3000172353, 0684-00-0576-01U; 10607567109633, 3000176574, 0684-00-0576-01U; 10607567109633, 3000176633, 0684-00-0576-01U; 10607567109633, 3000185680, 0684-00-0576-01U; 10607567109633, 3000196023, 0684-00-0576-01U; 10607567109633, 3000199196, 0684-00-0576-01U; 10607567109633, 3000199197, 0684-00-0576-01U; 10607567109633, 3000199198, 0684-00-0576-01U; 10607567109633, 3000200147, 0684-00-0576-01U; 10607567109633, 3000213850, 0684-00-0576-01U

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1686-2022%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.