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RNS-60 · news · pharmadog
← back to RNS-60
News mentioning RNS-60
25
stories
3d
Fresenius Kabi manufacturing plant hit with FDA warning letter after adverse events
biospace
5d
After GLP-1s, biosimilars are the new frontier in direct-to-employer plans
endpoints
11d
Convenience Kit Correction: Becton Dickinson Issues Correction for Kits and Procedure Trays Containing Recalled Sodium Chloride Ampules
fda medwatch
14d
Convenience Kit Correction: AVID Medical Issues Correction for Kits Containing Huons Sodium Chloride Ampules
fda medwatch
16d
Par Health Issues Voluntary Nationwide Recall of Two Lots of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection Due to the Presence of Particulate Matter
fda recalls
17d
Sodium Chloride Flush Recall: Spectra Medical Removes Sodium Chloride Injection USP Ampules
fda medwatch
18d
Otsuka ICU Medical LLC Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride Injection, USP Due To a Product Mix-up with 10 mEq Potassium Chloride Injection
fda recalls
25d
Epidural Kit Correction: Medical Action Industries Issues Correction for Epidural Kits Containing Spectra Medical Devices Lidocaine Ampules
fda medwatch
Sep 3, 26
B. Braun Medical Inc. Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container Due to the Presence of Particulate Matter
fda medwatch
Sep 2, 26
Early Alert: Convenience Kit Issue from AVID Medical
fda medwatch
Aug 27, 26
Convenience Kit Correction: AVID Medical Issues Correction for Kits Containing Medline Namic Star Off Handle Manifolds
fda medwatch
Aug 26, 26
Baxter Issues Voluntary Nationwide Recall for Two Lots of 0.9% Sodium Chloride Injection Due to Potential Presence of Particulate Matter
fda medwatch
Aug 21, 26
Early Alert: Epidural Kit Issue from Medical Action Industries
fda medwatch
Aug 18, 26
Early Alert: Convenience Kit Issue from Becton Dickinson
fda medwatch
Aug 11, 26
Fresenius Kabi Issues Nationwide Recall of Tyenne® (tocilizumab-aazg) Injection 400 mg/20 mL Vials Due to Presence of Glass Particles
fda medwatch
Aug 10, 26
FDA issues alert in wake of BD recall of faulty needle sets
fiercebiotech
Aug 5, 26
Fresenius Kabi Issues Voluntary Nationwide Recall of One Lot of Morphine Sulfate Injection, USP in a Simplist® Prefilled Syringe Due to Labeling Mix-up
fda medwatch
Aug 3, 26
Convenience Kit Correction: Medical Action Industries Issues Correction for Kits Containing Recalled Namic Manifolds
fda medwatch
Jul 30, 26
Convenience Kit Correction: Argon Medical Issues Correction for Convenience Kits Containing Spectra Medical Device Lidocaine Ampules
fda medwatch
Jul 16, 26
Opinion: The growing fang-to-pharmacy pipeline
stat
Jul 16, 26
Convenience Kit Correction: Arrow International Issues Correction for Convenience Kits Containing Recalled Huons Lidocaine and Bupivacaine and Saline
fda medwatch
Jul 9, 26
Early Alert: Convenience Kit Issue from Medical Action Industries
fda medwatch
Jul 7, 26
Infusion Pump Correction: Fresenius Kabi Issues Correction for Ivenix Large Volume Infusion Pump
fda medwatch
Jul 7, 26
Infusion Pump Correction: Fresenius Kabi Issues Correction for dropped or jarred Ivenix Large Volume Infusion Pumps
fda medwatch
Apr 27, 26
Trump administration warns against using federal dollars on fentanyl test strips
stat
