Methohexital Sodium Injection Recall
Methohexital Sodium for Injection 500 mg multiple dose vials made by OneSource Specialty Pharma have failed quality tests for impurities and degradation. …
ONESOURCE SPECIALTY PHARMA LIMITED
Every recall we are tracking for ONESOURCE SPECIALTY PHARMA LIMITED, newest first, sourced from the FDA. If you are wondering whether your ONESOURCE SPECIALTY PHARMA LIMITED product is recalled in 2026, check the list below for your model, lot, or VIN. Each entry explains the hazard and the free repair, replacement, or refund. Get a free email alert the moment a new ONESOURCE SPECIALTY PHARMA LIMITED recall posts.
1 recall · updated Jun 7, 2026
BD ChloraPrep Hi-Lite Orange applicators (a skin antiseptic) were distributed without proper sterilization assurance. These products should have been sterilized …
CareFusion 213, LLC
Methohexital Sodium for Injection 500 mg multiple dose vials made by OneSource Specialty Pharma have failed quality tests for impurities and degradation. …
ONESOURCE SPECIALTY PHARMA LIMITED
Lacosamide 100mg tablets made by Camber Pharmaceuticals may contain a different medication, Selexipag 1000 mcg, mixed into the bottle. Taking the wrong drug by …
Annora Pharma Private Limited
Gas-X Extra Strength Simethicone 125 mg softgels have been recalled because a machine leak during packaging may have contaminated the capsules with a diluted …
Haleon US Holdings LLC
Corlanor (ivabradine) 7.5mg tablets in 60-count bottles are being recalled due to the presence of a foreign substance. If you take this medication, stop and …
Amgen, Inc.
Corlanor (ivabradine) 5 mg tablets are being recalled because bottles may contain a foreign substance. If you take this medication, stop and contact your …
Amgen, Inc.
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