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Medos International Sarl is recalling Cerenovus CEREBASE DA Guide Sheath due to fractures in the distal catheter shaft where parts are joined.
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FDA Approves New Antibiotic for Three Different Uses
FDA Approves New Antibiotic for Three Different Uses
http://www.fda.gov/news-events/press-announcements/fda-approves-new-antibiotic-three-different-uses
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Teleflex and Arrow International Recall ARROW QuickFlash Radial Artery and Radial Artery/Arterial Line Catheterization Kits for Increased Resistance That May Lead to Vessel Injuries, Narrowing, or Blockage
ARROW QuickFlash Catheterization Kits are being recalled after reports of increased resistance with the guide wire and chamber during use.
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FDA Roundup: April 2, 2024
FDA Roundup: April 2, 2024
http://www.fda.gov/news-events/press-announcements/fda-roundup-april-2-2024
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AvKARE, LLC. Issues Voluntary Nationwide Recall of Atovaquone Oral Suspension, USP 750 mg/5 mL Due to Potential Bacillus Cereus Contamination
AvKARE, LLC. is voluntarily recalling lot # AW0221A of Atovaquone Oral Suspension, USP 750mg/5mL to the Consumer/User level, due to the potential Bacillus cereus contamination in the product found during stability testing at a 3rd party lab. Risk Statement: In the population most at risk, immunocom
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FDA Roundup: March 29, 2024
FDA Roundup: March 29, 2024
http://www.fda.gov/news-events/press-announcements/fda-roundup-march-29-2024
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Eugia US LLC (f/k/a AuroMedics Pharma LLC) Issues Voluntary Nationwide Recall of Methocarbamol Injection, USP 1000 mg/10 mL (100mg/mL) (Single Dose Vial) Due to Presence of White Particles
East Windsor, New Jersey, Eugia US LLC (f/k/a AuroMedics Pharma LLC) has initiated a voluntary recall of lot number 3MC23011 of Methocarbamol Injection, USP 1000 mg/10 mL (100mg/mL) (Single Dose Vial) – 10mL Vial to the consumer level due to a customer product complaint for the presence of white par
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Amneal Pharmaceuticals, LLC. Issues a Nationwide Voluntary Recall of Vancomycin Hydrochloride for Oral Solution USP, 250mg/5mL, Due to the Potential for Some Bottles to be Super Potent Which May be Harmful
Amneal Pharmaceuticals, LLC. Bridgewater, New Jersey (Amneal), is voluntarily recalling 4 lots (see table below) of Vancomycin Hydrochloride for Oral Solution, USP, 250 mg/5mL packaged in 80 mL, 150 mL, or 300 mL pack sizes, to the Consumer Level. Some bottles may have been overfilled which can res
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FDA Roundup: March 26, 2024
FDA Roundup: March 26, 2024
http://www.fda.gov/news-events/press-announcements/fda-roundup-march-26-2024
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FDA Warns Consumers to Avoid Certain Topical Pain Relief Products Due to Potential for Dangerous Health Effects
FDA Warns Consumers to Avoid Certain Topical Pain Relief Products Due to Potential for Dangerous Health Effects
http://www.fda.gov/news-events/press-announcements/fda-warns-consumers-avoid-certain-topical-pain-relief-products-due-potential-dangerous-health