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381. Coastal Meds recalls all drug products marketed as sterile
The FDA is alerting healthcare professionals to a voluntary recall of all sterile injectable products made by Coastal Meds, a compounding pharmacy based in Biloxi, Miss. While the company issued the ...17 April 2018 -
382. Your hospital costs aren’t as fixed as you think: Uncovering hidden savings
... groups acquire a new group or location, and ask our help to integrate the facilities and develop the best costs portfolio for a merged formulary.” Kalinowski recalls some healthcare clients whose savings ...28 March 2018 -
383. There are more people living with Aphasia than we thought: How to change policies, procedures & care
... all faced a heavy future. Sarah recalls, “My dad felt guilty. Everyone felt uncertain. After my dad moved in, we felt stuck, afraid and just thrown to the wolves. I was preparing to quit my job to care ...20 March 2018 -
384. Bayer recalls Alka-Seltzer Plus products over packaging issues
Bayer recalled some Alka-Seltzer Plus products after discovering ingredients listed on the package's front sticker may differ from the product's actual ingredients. The recall applies to Alka-Seltzer ...19 March 2018 -
385. Hospira recalls opioid due to cracked vials: 4 things to know
Hospira recalled three lots of Hydromorphone HCl injection Feb. 7 after discovering the glass vials containing the opioid could be cracked or empty, according to a March 5 recall alert from the FDA. Here ...07 March 2018 -
386. 6 ways health systems can drive revenue and reduce costs through strong supplier partnerships
... and a patient outcome perspective." Mr. Eastham recalls speaking with the director of pharmacy services at a single hospital system who expressed frustration in having to toggle between 16 disparate ...28 February 2018 -
387. FDA declares Class I recall for 48 Medtronic defibrillators
The U.S. Food and Drug Administration declared a Class I recall of 48 Medtronic defibrillators due to a manufacturing defect. Class I recalls indicate the devices may cause serious injuries or death, ...27 February 2018 -
388. 3M recalls surgical warming blankets
3M Co. recalled 33,108 cases of its underbody warming blankets used to keep patients warm during surgery, according to an FDA safety alert issued Feb. 12. The company recalled its Bair Hugger underbody ...20 February 2018 -
389. Philips recalls HeartStart MRx Defibrillator: 3 things to know
Philips recalled its HeartStart MRx Defibrillator due to an equipment defect, according to a Feb. 9 safety notice from the FDA. Here are three things to know. 1. Philips initiated the recall in June ...13 February 2018 -
390. Report: Software issues continue to drive medical device recalls in Q4
Software issues constituted the No. 1 reason for U.S. medical device recalls for the seventh consecutive quarter, according to a recent analysis of 2017 fourth-quarter recall data. Each quarter, product ...09 February 2018