Bard Peripheral Vascular PowerPort duo M.R.I recall — FDA Z-1551-2021
Catheters may experience difficulty in flushing, infusion, and/or aspiration, and septum dislodgements.
Complete FDA and NHTSA recall records dated in May 2021.
These records include useful source details for the selected month.
Catheters may experience difficulty in flushing, infusion, and/or aspiration, and septum dislodgements.
Emergency Use Application (EUA) application withdrawn as false negative results reported
Due to molding defect, there is a potential that certain lots of spinning and non-spinning Sprios male luers may exhibit small amounts of leakage in the inactivated position.
GE Healthcare has become aware of a potential issue on 800 family NM/CT Scanners that could cause a shift in CT radiation exposure range of up to 5cm compared to the intended radiation…
Due to molding defect, there is a potential that certain lots of spinning and non-spinning Sprios male luers may exhibit small amounts of leakage in the inactivated position.
ReWalk Robotics received two complaints (one in the US; one in the Germany), which alleged that the ReWalk device waistpack (which is the location of the Li-Ion battery packs) caught fire…
Due to molding defect, there is a potential that certain lots of spinning and non-spinning Sprios male luers may exhibit small amounts of leakage in the inactivated position.
Catheters may experience difficulty in flushing, infusion, and/or aspiration, and septum dislodgements.
Due to molding defect, there is a potential that certain lots of spinning and non-spinning Sprios male luers may exhibit small amounts of leakage in the inactivated position.
Due to a manufacturing issue associated with the mixing process of the epoxy used in the manufacture of pacemaker from years 2015 through 2018, the affected devices may malfunction caused…
Bezel repair parts used, not by the original manufacturer, to service and repair infusion pump modules, may over time experience cracking or separation of the posts from the bezel. The…
Bezel repair parts used, not by the original manufacturer, to service and repair infusion pump modules, may over time experience cracking or separation of the posts from the bezel. The…
Due to molding defect, there is a potential that certain lots of spinning and non-spinning Sprios male luers may exhibit small amounts of leakage in the inactivated position.
Due to molding defect, there is a potential that certain lots of spinning and non-spinning Sprios male luers may exhibit small amounts of leakage in the inactivated position.
The Hershey Company, 19 East Chocolate Avenue, Hershey PA 17033 is voluntarily recalling of a specific lot of Hershey s Chocolate Shell Topping in a 7.25-oz. (205g) bottle UPC (346000)…
Notified by packaging supplier of recall due to potential loose particles of CPET in product packaging that could become imbedded in the finished baked goods.
Firm determined that pesticide Bifenazate MRL is out of compliance for the US market. US MRL = 5ppm. Product tested = 5.8ppm.
The firm was notified by its ingredient supplier of Medium Chain Triglycerides (MCT) that the ingredient potentially contained traces of milk. This affected two of the firm's products that…
Incorrect active ingredient is listed on product label
The firm was notified by an ingredient supplier of Medium Chain Triglycerides (MCT) that the ingredient potentially contained traces of milk. This affected two of the firm's products that…
Presence of foreign substance: identified as activated carbon.
Defective Delivery System: An increase in complaints identified endcap being loose or falling off upon activation releasing glass shards containing the solution.
Incorrect size printed on the device; packaging is labeled correctly.
When the Cross Enterprise Display option is enabled on the Centricity Universal Viewer and Workflow Manager option is used as the PACS worklist launching the viewer, the patient jacket may…
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.