Concentrated coffee packed in 1/2 gallon or 1 gallon hermetically sealed Scholle or Liquibag.
Liquid Coffee
The pH level in coffee product was elevated above 4.6.
95,094 total recalls in our database
Liquid Coffee
The pH level in coffee product was elevated above 4.6.
Tarry Medical Products
Microbial contamination
Product failed to meet air space specifications
Texas Star Nut and Food Co.
Potential to be contaminated with Salmonella.
Product failed to meet air space specifications
The chocolate used in the product contains vanillin (an artificial ingredient) but is labeled to contain vanilla.
Bliss Bros Dairy
Product failed to meet air space specifications
Undeclared soy lecithin in 5 dietary supplements.
Texas Star Nut and Food Co.
Potential to be contaminated with Salmonella.
A natural flavoring containing a milk ingredient was inadvertently used to manufacture the Duncan Hines Signature Swiss Chocolate Cake Mix, 16.5 oz. cartons and the Duncan Hines Swiss Moist Deluxe Swiss Chocolate (Chocolate Suizo) 16.5 oz. cartons. The incorrect labeling was used on this product declaring that these products were a NON-milk containing product.
Bliss Bros Dairy
Product failed to meet air space specifications
Bliss Bros Dairy
Product failed to meet air space specifications
Mckesson Packaging Services
Labeling: Label mix-up -outer carton incorrectly labeled as aspirin chewable tablets.
Incorrect Power Supply in the package, rendering the device inoperable.
The label on the Tyvek bag is missing. This is used by customers to identify material code, lot number, and expiration date once the product is removed from the shipper box.
Complaints of false positive HET mutations and leaking cards; could lead to unnecessary invasive testing during pregnancy and the associated risks of such invasive testing.
GE Medical Systems
The vacuum suction tubing could be kinked within the machine resulting in suction less than the 20 lpm required by ISO 10079-3. This could result in inadequate suction performance to clear the airway and inadequate ventilation of the patient.
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Medtronic is conducting a voluntary Urgent Medical Device Recall of two lots of the PowerCross 0.018" ¿ Over the Wire (OTW) Percutaneous Transluminal Angioplasty (PTA) Dilatation Catheter because the product is mislabeled.
Potential disassociation of the orientation pin.
Firm's quarterly dose audit testing showed that one batch was radiated below the augmented dose and therefore did not meet the augmented dose of 28.4 kGy.