Purely Pomegranate GOKNUR Organic Frozen/IQF Pomegranate Arils recall — FDA F-1673-2014
Purely Pomegranate, Inc. is voluntarily recalling frozen IQF pomegranate arils due to public concerns about the Hepatitis A Virus.
Complete FDA and NHTSA recall records dated in 2014, organized for browsing by month, category and recalling company.
Select a month to review the recall records reported during that period.
Records are ordered by the best available source date.
Purely Pomegranate, Inc. is voluntarily recalling frozen IQF pomegranate arils due to public concerns about the Hepatitis A Virus.
Gretchen's Shoebox Express is recalling Greek Yogurt Raspberry & Lemon Parfait cups sold under the Starbucks brand due to undeclared egg.
Due to the lack of the ingredient statement the firm failed to declare the following direct allergens: peanuts, tree nuts, soy, wheat, and yellow #5. The products also lack the declaration…
Due to the lack of the ingredient statement the firm failed to declare the following direct allergens: peanuts, tree nuts, soy, wheat, and yellow #5. The products also lack the declaration…
Tortillas Mexico is recalling all tortillas with the Expiration Dates from December 20 to February 27, 2014 because a meatal staple was found by a consumer in a baked tortilla.…
Tortillas Mexico is recalling all tortillas with the Expiration Dates from December 20 to February 27, 2014 due to metal detector malfunction during production and therefore potential for…
Tortillas Mexico is recalling all tortillas with the Expiration Dates from December 20 to February 27, 2014 because a meatal staple was found by a consumer in a baked tortilla.…
Contains undeclared wheat
All American Seasonings is recalling T3695 White cheddar jalapeno seasoning powder, lots 34577 and 40257 after being notified by Elite spice that there was a potential recall for salmonella…
Presence of Particulate Matter: Particulate matter includes wood, sodium citrate and dextrose.
Presence of Foreign Matter: Guaifenesin API powder is being recalled due to the possibility that the product contains polyethylene fibers from a screen used to sift the Guaifenesin.
Presence of Particulate Matter: Particulate matter includes wood, sodium citrate and dextrose.
Presence of Particulate Matter: Units of this lot may have visible metal particles embedded in the vial and in the solution causing the product to be discolored.
Crystallization; visible crystals from the active ingredient formed due to extreme cold temperatures during shipping
Presence of Particulate Matter: Baxter is issuing a voluntary recall for these IV solutions due to particulate matter found in the solution identified as polyester and cotton fibers,…
Presence of Particulate Matter: Particulate matter includes wood, sodium citrate and dextrose.
Defective Delivery System: Out of Specification (OOS) results for the z-statistic value, which relates to the patients and caregiver ability to remove the release liner from the patch…
Failed Dissolution Specification: Out of Specification dissolution results at 12 month interval.
Presence of Paticulate Matter; Baxter is issuing a voluntary recall for these IV solutions due to particulate matter found in the solution identified as polyester and cotton fibers,…
Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the FDA has determined that the products was found to contain sildenafil, an undeclared active pharmaceutical…
Defective Delivery System: Out of Specification (OOS) results for the z-statistic value, which relates to the patients and caregiver ability to remove the release liner from the patch…
Global Vitality is recalling dietary supplements because they may be contaminated with chloramphenicol. The dietary supplements were made with a raw ingredient that was on recalled by…
Presence of undeclared allergens soy, and milk
Charlemagne's Tree Farm, Ltd. dba HUDSON VALLEY HOMESTEAD recalled BUSHWHACKER'S Savory Sauce Mild and Hot & Spicy due to Undeclared Anchovies.
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.