Sources

FDA MedWatch

• Manual Resuscitator Recall: Ambu Inc. Removes SPUR II Resuscitators Due to Blocked Manometer Port 16 hours 44 min old
• Green Lumber Holding, LLC Issues Consumer Alert on Counterfeit Products Following FDA Findings 16 hours 44 min old
• DermaRite Industries Expands Voluntary Nationwide Recall Due to Potential Burkholderia cepacia Contamination 1 day 16 hours old

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Quality and Safety in Health Care Journal

• Correction: Its time for the field of geriatrics to invest in implementation science 1 week 4 days old
• Why tackling overuse will not succeed without changing our culture 1 week 4 days old
• Unreasonable effectiveness of training AI models locally 1 week 4 days old

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Google Groups

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Institute for Healthcare Improvement

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Journal for Healthcare Quality

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Journal of Patient Safety

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