Mini Resupply Trauma Kit - Product Code 85-0835, North American Rescue
North American Rescue
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
💊 Drugs • 3,313 recalls
North American Rescue
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
North American Rescue
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
North American Rescue
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
North American Rescue
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Cadila Pharmaceuticals Limited
Microbial Contamination of Non-Sterile Product
Failed Stability Specifications; out-of specification value for homogeneity / phase separation.
GSK Consumer Healthcare
Labeling Not Elsewhere Classified: front labels have the incorrect NDC or 0145-1506-01 instead of the correct NDC of 0145-1506-05 and some back labels have the incorrect indication stating "use for the cure of most jock itch" rather than "use for the cure of most athlete's foot".
Subpotent Drug: Out of Specification assay values on stability for the active ingredient, zinc pyrithione.
Subpotent Drug: concentration of product is less than labeled amount.
Pharmedium Services
Stability Data Does Not Support Expiry: potential loss of potency in drugs packaged and stored in syringes.
The Harvard Drug Group
Microbial contamination of Non-Sterile Products; positive findings of Burkholderia cepacia
Pharmedium Services
Stability Data Does Not Support Expiry: potential loss of potency in drugs packaged and stored in syringes.
Pharmacy Plus, Inc.
Lack of Assurance of Sterility
CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.
CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.
CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.
CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.
Pharmacy Plus, Inc.
Lack of Assurance of Sterility
CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.
CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.