Fentanyl Citrate and Bupivacaine HCl in 0.9% Sodium Chloride in all strengths
Lack of sterility assurance.
Class II means the product may cause temporary or medically reversible harm, and serious harm is unlikely. It is by far the largest recall class - most potency, dissolution and labeling problems land here.
14,543 recalls, newest first.
Lack of sterility assurance.
Lack of sterility assurance.
Lack of sterility assurance.
Lack of sterility assurance.
Temperature Abuse: Complaints of tablets being wet and stuck together with tablet coating peeled and disintegrated as a result of prolonged exposure to high temp during distribution.
Lack of Assurance of Sterility: Leakage of the peritoneal dialysis (PD) solution bag.
Failed Stability Specifications:stability failure at 12 months, long term RT conditions.
Failed Stability Specifications:stability failure at 12 months, long term RT conditions.
Cross Contamination With Other Products: metronidazole powder was found in one bottle of Divalproex Sodium.
Presence of particulate matter
Presence of Particulate Matter: identified as polyethylene, which is consistent with the material used to manufacture the contain cap
Failed Stability Specifications
GMP Deviations: manufacturing of API material did not meet GMP and quality requirements.
GMP Deviations: manufacturing of API material did not meet GMP and quality requirements.
GMP Deviations: manufacturing of API material did not meet GMP and quality requirements.
GMP Deviations: manufacturing of API material did not meet GMP and quality requirements.
GMP Deviations: manufacturing of API material did not meet GMP and quality requirements.
Failed Impurities/Degradation Specifications: High out of specification test result for the Moexipril Diketopiperazine impurity was obtained during routine stability testing.
Failed Stability Specifications: Product stability testing results did not meet specifications for iron content.
Microbial Contamination of Non-Sterile Products: potentially contamination with the bacteria Burkholderia cepacia
Defective Container: products showed leakage (bubbles, foaming) of propellant and product from the container valve cup area.
Defective Container: products showed leakage (bubbles, foaming) of propellant and product from the container valve cup area.
Defective Container: products showed leakage (bubbles, foaming) of propellant and product from the container valve cup area.
Labeling: Incorrect or Missing Lot and/or Exp Date - product label was missing lot number and beyond use date.
Labeling: Label Mix-Up.some bottles labeled as Gabapentin 800 mg contain Gabapentin 600 mg