Medscape2d
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 ...
foodengineeringmag5d
US Product Recalls Reach Second-Highest Level Over Six Years in 2024
The food and drink industry faced several major recalls in 2024, driven by safety risks, such as lead-contaminated cinnamon ...
GlobalData on MSN3d
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 specific environmental settings allowing the growth of the fungus Aspergillus ...
Ransomware Hacked & Helpless
On January 23, the dark web erupted with a fresh claim, as BASHE, a shadowy ransomware group with a reputation for striking ...
aha.org1d
ICU Medical recalls certain lots of potassium chloride injection bags due to mislabeling
The Food and Drug Administration Feb. 18 announced that ICU Medical is voluntarily recalling certain lots of its potassium ...
MassDevice6d
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 ...
ConsumerAffairs5d
ICU Medical recalls potassium chloride injection bags due to mislabeling error
ICU Medical has issued a voluntary recall of Potassium Chloride Injection 20 mEq, packaged in 100 mL bags, due to incorrect overwrap labels stating 10 mEq instead of 20 mEq. The recall focuses on ...
Monthly Prescribing Reference1d
Fungus Concerns Prompt Recall of Surgical Prep Product
Becton, Dickinson and Company (BD) is recalling 1 lot of ChloraPrep™ Clear 1 mL Applicators due to the potential for fungal contamination. According to ...
Local 12 WKRC Cincinnati5d
Nearly 100,000 bottles of nasal spray recalled for 'microbial failure'
The product was first recalled by the company in December of 2024 with a letter to customers titled "URGENT: MEDICAL DEVICE RECALL," but the FDA only recently issued its recall. The FDA said ...
Yahoo Finance6d
ICU Medical Issues Nationwide Recall of POTASSIUM CHLORIDE INJECTION, 20 mEq and POTASSIUM CHLORIDE INJECTION, 10 mEq Due to Mislabeling
LAKE FOREST, Ill., Feb. 13, 2025 /PRNewswire/ -- ICU Medical, Inc. is voluntarily recalling one lot each of POTASSIUM CHLORIDE Inj. bags with overwrap labels 10 mEq, packaged in cases of POTASSIUM ...
New York Post4d
Quaker Oats pancake mix recall upgraded to highest risk level over threat of ‘life-threatening allergic reaction’
Officials from the Food and Drug Administration (FDA) recently escalated the recall of certain Quaker Oats pancake mixes earlier this week, increasing the recall category to the most serious level.
Fox Business4d
Quaker Oats recall updated to 'most serious' category as FDA sounds alarm on pancake mix
Officials from the Food and Drug Administration (FDA) recently escalated the recall of certain Quaker Oats pancake mixes earlier this week, increasing the recall category to the most serious level.