FDA recalls 90K bottles of nasal spray due to potential ‘adverse’ effects: Throw out ASAP
The recalled products were sold across 32 states — including Massachusetts, Connecticut, Rhode Island and Vermont.
ConsumerAffairs16h
Fewer products recalled in 2024 despite elevated recall announcements
The number of recalls stayed high in 2024 but fewer units of products got recalled. There were 3,232 product recalls in 2024, ...
Medscape17h
Urgent Recall for Abiomed Heart Pumps
Abiomed has issued an Urgent Medical Device Correction updating the instructions for its Impella RP with SmartAssist and also its Impella RP Flex with SmartAssist heart pumps. The US Food and Drug ...
Nearly 100,000 bottles of nasal spray recalled for 'microbial failure'
Almost 100,000 bottles of nasal spray were recalled for a "microbial failure" that led to multiple complaints from customers.
Why Quaker Oats Waffle Recall Set To FDA’s Highest Risk Level
FDA updates Quaker Oats' pancake & waffle mix recall to Class I, its highest risk level, due to undeclared milk. Check if ...
Becker's Hospital Review11d
4 recent medical device recalls and corrections
JIANGSU JUMAO X-CARE Medical Equipment Co. issued a recall for the JMC5A Ni/Tru-Aire-5 Oxygen Concentrator after incidents of spontaneous fires. These fires could cause burns or worse. Patients are ...
GlobalData on MSN1d
BD recalls ChloraPrep applicators lot over fungal contamination
BD has announced a voluntary worldwide recall of a single lot of ChloraPrep Clear 1mL applicators over contamination under ...
MassDevice4d
J&J’s Abiomed updates Impella RP instructions in Class I recall
The FDA today issued a notice informing customers of updated instructions for the Johnson & Johnson Abiomed Impella RP heart ...
pharmaphorum18d
Device ad-vice: Best practices for handling a medical device recall
On the bright side, AdvaMed, a global device manufacturer advocacy organization, recently stated that less than one percent of devices cleared since 1998 were involved in Class I recalls 5.
HME News12d
Urgent recall issued for TrueAire-5 oxygen concentrator
The U.S. Food and Drug Administration has issued an urgent recall for the JMCC5A Ni/TruAire-5 Oxygen Concentrator due to the device spontaneously catching fire.
MedPage Today23d
Limbo of Cardiac Device Recalls Has Physicians Ready for Change
A recent study identified 157 cardiovascular devices recalled from 2013 to 2022. Recalls were commonly attributed to device design (31.4%), process control (16.1%), or component design or ...
NL Times6h
Philips suffered €698 million loss last year, mainly over $1.1 billion recall settlement
Philips ended 2024 deep in the red, suffering a loss of 698 million euros, the health tech company announced on Wednesday.