
Bacteria Contamination Leads to Recall of Cold Relief Medications
Ninjacof and Ninjacof A: Recall — potential Burkholderia cepacia contamination. ISSUE: Centurion Labs is voluntarily recalling 1 lot of Ninjacof (Lot# 200N1601) and 1 lot of Ninjacof A (Lot# 201NA1601) manufactured by Vilvet and distributed by Centurion Labs to the retail level due to potential contamination with Burkholderia cepacia. Centurion was notified by the FDA…
Sterility Concerns Lead to Recall of Numerous Unexpired Products
Pravastatin Sodium Tablets Packaged in Bottles Recalled
Pravastatin sodium tablets by International Laboratories: Recall—mislabeling. ISSUE: International Laboratories, LLC is voluntarily recalling one (1) Lot of Pravastatin Sodium Tablets USP 40 mg packaged in bottles of 30 tablets, to the consumer level due to mislabeling. The product is labeled as Pravastatin Sodium Tablets USP 40 mg but contained Bupropion Hydrochloride XL 300 mg…
FDA Investigating Serious Adverse Events Involving Compounded Curcumin
Possible Contamination Triggers Recall of Some Rugby Labs Products
Possible Mislabeling of Tablets as Capsules Leads to Voluntary Recall
FDA Warns of Adverse Reactions to Compounded Intravitreal Eye Injection Drug
Anabolic Steroid Derivatives Lead to Dietary Supplement Recall
Lack of Sterility Assurance Leads to Secondary Recall of Syringe
Succinylcholine Chloride 20mg/mL 5mL syringe by Fagron Sterile Services: Recall—potential lack of sterility assurance. ISSUE: Fagron Sterile Services is voluntarily recalling three (3) lots of Succinylcholine Chloride 20mg/mL 5mL syringe to the hospital/clinic level. The secondary recall of product manufactured by Hospira Inc., a Pfizer company, and repacked by Fagron Sterile Services, is due to…








