Foreign material (plastic pieces)
All Recalls
95,102 total recalls in our database
FG21004 Brussels Sprouts, Roasted 2514111 FG21004 Brussels Sprouts, Roasted 2514311 Packaged 7- 2 lb polybags per cardboard case
AND GO CONCEPTS
Potential to be contaminated with Listeria monocytogenes
Foreign material (plastic pieces)
Potential Listeria Monocytogenes Contamination
FG20007 Pepper, Red Bell Chop packaged in poly bag, and cardboard case. 17.5 lbs per case
AND GO CONCEPTS
Potential to be contaminated with Listeria monocytogenes
Potential Listeria Monocytogenes Contamination
Potential Listeria Monocytogenes Contamination
Pasteurized Donor Human Milk , 4oz plastic bottle
Henry Ford Milk Bank- Jackson
Foreign material (plastic particulate from outer closure) between immediate closure (foil seal) and outer closure (plastic cap)
Aunt Mid's Fresh Sliced Mushrooms 227g (8 oz.) BEST BEFORE 25JL04 MEILLEUR AVANT, UPC 0 33383 676005 on top and best before date of BEST BEFORE 25JL04 stamped on side, 12 packages per case
Wiet Peeters Farm Products Limited
Potential to be contaminated with Listeria monocytogenes
Foreign material (plastic)
Potential Listeria Monocytogenes Contamination
Foreign material (plastic pieces)
Product Mix Up: This product is being recalled because of a complaint received that a sealed bottle of lisinopril and hydrochlorothiazide tablets 20mg/12.5 mg had a foreign tablet identified as atazanavir and ritonavir tablet 300mg/100mg.
Subpotent Drug: Assay below the approved specification
PERIPHERAL PARENTERAL NUTRITION, Compounded Sterile Preparation, Refrigerated Injection, Rx Only, Single Dose Injection, a) 1440 mL bag, b) 1700 mL bag, Central Admixture Pharmacy Services, Inc, Los Angeles, 13128 Imperial Hwy, Santa Fe Spr., CA 90870.
Central Admixture Pharmacy Services, Inc (CAPS) Los Angeles
Lack of Processing Controls; prescriptions were compounded in an ISO-5 area where it was identified that a daily cleaning step was not sufficiently documented.
CGMP Deviations: detection of N-nitroso-dimethyl-rizatriptan impurity, above the FDA recommended acceptable intake limit.
Subpotent Drug: Assay below the approved specification
Labeling: Incorrect or Missing Lot and/or Exp. Date: A printing issue resulted in incorrect lot numbers on the label.
Presence of foreign tablets/capsules: presence of foreign Divalproex Sodium Extended-Release 250mg tablet in a bottle of omeprazole capsules.
CGMP Deviations