Optisite Arterial Cannula recall — FDA Z-2080-2025
due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.
Browse the newest complete recall records currently stored from FDA enforcement reports and NHTSA vehicle campaigns. “Latest” refers to the newest source-dated record in this database, not the timestamp of our last API check.
The newest recall records with useful source details are listed here.
due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.
May be contaminated with fluid from a reach truck
Product is likely Canola Oil, not Extra Virgin Olive Oil
May be contaminated with fluid from a reach truck
May be contaminated with fluid from a reach truck
Potential to be contaminated with Listeria monocytogenes
Label declares Shelled Edamame but does not specify or declare soy.
May be contaminated with fluid from a reach truck
May be contaminated with fluid from a reach truck
May be contaminated with fluid from a reach truck
Product may contain foreign objects of metal origin.
Undeclared milk
Contains undeclared colors (FD&C Blue 1 and FD&C Red 40)
cGMP deviations
cGMP deviations
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
Presence of Foreign Substance- Black hair strand found attached to a tablet in a sealed bottle.
cGMP deviations
Ford Motor Company (Ford) is recalling certain 2021-2024 Bronco Sport and 2020-2022 Escape vehicles equipped with 1.5L engines. A fuel injector may crack and leak fuel inside the engine…
Products have the incorrect platelet (PLT) value assignments for the ADVIA 120/2120/2120i Hematology Systems.
Ultrasound transducer devices were refurbished beyond their useful life.
Multiple plate failures documented as a result of the Low Positive Template Control being too high and out of range using the affected lot of ColoSense Test Kit.
A software anomaly allows test results to be reported using Micro Tip and Micro Slide diluent packs that the system treats as expired even when the Use Expired Reagents setting is not…
Medline Industries, LP. is issuing a recall for specific Medline kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN which was identified that during insertion of the…
Browse recent months with enough recall history for useful comparison.