Manufacturer
291 recalls in our database name PharMEDium Services, LLC. as the manufacturing or recalling firm.
Of the 291 recalls from PharMEDium Services, LLC. we have scored against our rubric, 8 (3%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 196 (67%) are Severe.
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
PharMEDium Services is recalling 499 syringes of Hydromorphone HCl injection because the product failed potency specifications.
Pharmedium Services, LLC is voluntarily recalling 60 bags of compounded Oxytocin injection because the drug was found to be subpotent.
Pharmedium Services is voluntarily recalling 42 bags of compounded Oxytocin 40 units in Lactated Ringer's solution because the drug was subpotent.
Pharmedium Services, LLC is voluntarily recalling 763 bags of compounded Oxytocin 30 units in Lactated Ringer's USP. The recall was initiated because the drug was found to be subpotent.
Pharmedium Services, LLC is voluntarily recalling 4,452 bags of compounded Oxytocin 30 units due to subpotent drug levels. The FDA classified this as a Class II recall.
Pharmedium Services, LLC is voluntarily recalling 564 bags of compounded Oxytocin 10 units in Lactated Ringer's Injection because the drug was subpotent.
Pharmedium Services, LLC is recalling 1,308 bags of compounded Oxytocin 10 units in Lactated Ringer's Injection because the drug was subpotent.
Pharmedium Services, LLC is voluntarily recalling 90 bags of compounded Oxytocin 40 units in Lactated Ringer's because the drug was subpotent.
Pharmedium Services, LLC is voluntarily recalling 2,232 bags of compounded Oxytocin injection because the drug was found to be subpotent.
Pharmedium Services, LLC is voluntarily recalling Oxytocin 20 units in Lactated Ringer's Injection USP bags because the drug was found to be subpotent.
Pharmedium Services is recalling 6,108 bags of compounded Oxytocin 30 units in Lactated Ringer's because the drug was subpotent. The recall is voluntary and nationwide.
Pharmedium Services, LLC is voluntarily recalling 24,486 bags of compounded Oxytocin 30 units in Lactated Ringer's because the drug was subpotent.
Pharmedium Services, LLC is voluntarily recalling 534 bags of compounded Oxytocin 30 units in 1000 mL bags because the drug was found to be subpotent.
Pharmedium Services, LLC is voluntarily recalling 1,152 bags of compounded Oxytocin 40 units in Lactated Ringer's USP because the drug was subpotent.
Pharmedium Services, LLC is voluntarily recalling 390 bags of compounded Oxytocin 20 units in Lactated Ringer's Injection due to subpotent drug levels.
Pharmedium Services, LLC is voluntarily recalling 978 bags of compounded Oxytocin in Lactated Ringer's Injection because the drug was subpotent.
PharMEDium Services is recalling 590 bags of compounded Fentanyl Citrate because the diluent used was expired before the product's assigned expiration date.
PharMEDium Services is recalling 295 bags of compounded Fentanyl Citrate because the diluent used was expired before the product's assigned expiration date.
PharMEDium Services is recalling specific lots of Potassium Phosphate Injection due to a media fill failure that compromised sterility assurance.
PharMEDium Services is recalling specific lots of Potassium Phosphate in 5% Dextrose Injection due to a media fill failure that compromised sterility assurance.
PharMEDium Services is recalling specific lots of Potassium Phosphate in 0.9% Sodium Chloride Injection due to a media fill failure that compromised sterility assurance.
PharMedium Services is recalling specific lots of Potassium Phosphate in 5% Dextrose Injection due to a media fill failure that compromised sterility assurance.
PharMEDium Services is recalling specific lots of Potassium Phosphate in 0.9% Sodium Chloride Injection due to a media fill failure at the manufacturer that raises concerns about sterility.
PharMEDium Services is recalling specific lots of Potassium Phosphate Injection due to a media fill failure that raises concerns about sterility.
PharMedium Services is recalling specific lots of Succinylcholine Chloride Injection due to a media fill failure that compromised sterility assurance.