Pilling COOLEY SUMP-SUCTION TUBE, REF 351547
FDA Recall Z-0846-2019 · Posted None
Advertisement
Recalling FirmTeleflex Medical
Recall StatusTerminated
Product CodeJOL
Date Initiated2019-01-07
Date Terminated2021-11-04
Product Quantity80 units
Reason for Recall
The internal tip is missing from the device, causing the device to not function as intended.
Firm Action
The firm initiated the recall by letter on 01/07/2019. The firm requested the return of the units.
Root Cause
Nonconforming Material/Component
Distribution Pattern
TX, NY, DC and Philippines
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
Advertisement