FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Let's Do Lunch, Inc.
- Product
- Integrated Food Service Chicken Little Sliders-Wrapped Cod…
- Reason
- Potential Listeria monocytogenes contamination.
- Published
- August 17, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Let's Do Lunch, Inc.
- Product
- Integrated Food Service Italian Submarine Sandwich Code #C…
- Reason
- Potential Listeria monocytogenes contamination.
- Published
- August 17, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Let's Do Lunch, Inc.
- Product
- Cafe Favorites Oven Roasted Turkey Breast & Cheese Melt on…
- Reason
- Potential Listeria monocytogenes contamination.
- Published
- August 17, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Let's Do Lunch, Inc.
- Product
- Cafe Favorites Oven Roasted Turkey Breast & Cheese Deli Fla…
- Reason
- Potential Listeria monocytogenes contamination.
- Published
- August 17, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Let's Do Lunch, Inc.
- Product
- Integrated Food Service Turkey Breast & Cheese Sandwich on…
- Reason
- Potential Listeria monocytogenes contamination.
- Published
- August 17, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Betamethasone Acetate / Betamethasone Sodium Phosphate Injectable Suspension, 7 mg/ mL,10 mL Multi-Dose vial for injection, Rx Only, Isomeric Pharmacy Solution, 2401 Foothill Dr., Salt Lake City, UT 84109
by Isomeric Pharmacy Solution, LLC
- Reason
- Lack of processing controls: Isomeric Pharmacy Solution, LLC is recalling Betamethasone Acetate / Betamethasone Sodium Phosphate 7 mg/mL INJ SUSP because of the potential of drug clumps in the vial of the sterile drug product and larger particle sizes.
- Published
- August 10, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Children's Qnasl 40 mcg (beclomethasone dipropionate) Nasal Aerosol, 40 mcg per spray, 60 Metered Sprays per canister, 4.9g Net Contents, Rx only; Professional Sample; Manufactured for Teva Respiratory, LLC, Horsham, PA 19044; By: 3M Drug Delivery Systems, Northridge, CA 91324; NDC 59310-206-08.
by Teva North America
- Reason
- Failed Content Uniformity Specifications: out of specification test result for spray content uniformity.
- Published
- August 10, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Oxygen Nasal Wash (purified water, xylitol, stabilized oxygen, sodium chloride) solution, .75 oz (22mL) bottle, Distributed by: Let's Talk Health, Chula Vista, CA 91914.
by Let's Talk Health, Inc.
- Reason
- Marketed Without An Approved NDA/ANDA: product is an unapproved drug due to nasal decongestant claims as well as not complying with the nasal decongestant final monograph.
- Published
- August 10, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
S-L Snacks NC, LLC
- Product
- Lance Oyster Crackers, Dist. by Snyder's-Lance, Inc., Charlo…
- Reason
- May contain low levels of peanut residue.
- Published
- August 10, 2016
- Distribution
- AL, FL, GA, IL, IN, IA, KS, KY, LA, MD,…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Inner Health Group, Inc dba Michael's Naturopathic Programs
- Product
- Michael's Naturopathic Programs Cholesterol Metabolism Facto…
- Reason
- May contain undeclared milk (in the form of calcium caseinate) and soy.
- Published
- August 10, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
The Kroger Co
- Product
- Kroger DELUXE ICE CREAM S'MORES 48 FL OZ (1.5 QT) 1.4 ML ING…
- Reason
- The firm was notified that the product was manufactured with an ingredient that may contain low levels of peanut reside which is not declared in the ingredient statement.
- Published
- August 10, 2016
- Distribution
- Product was shipped to the following sta…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Ach Food Companies Inc
- Product
- Salad topping labeled under the following brand names: (Pr…
- Reason
- Product manufactured with ingredient which may be contaminated with Listeria monocytogenes.
- Published
- August 10, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Honey Bunchie, LLC
- Product
- Honey Bunchies Gourmet Honey Bars, 1.9 oz. snack bar contain…
- Reason
- Honey Bunchie, LLC is initiating a voluntary recall of a limited number of Honey Bunchies Gourmet Honey Bars that contain SunOpta sunflower kernels that have the potential of contamination with Listeria monocytogenes.
- Published
- August 10, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Club Chef LLC
- Product
- Diced and sliced yellow onions. 2.5 lb & 5 lb clear plastic…
- Reason
- The firm was notified by a customer that the whole uncut product test positive for Listeria
- Published
- August 10, 2016
- Distribution
- Product was shipped to the following sta…
View recall →
FDA Recall
Terminated
Historical recordClass III
mitoXANTRONE Injection USP (concentrate), 20 mg/10 mL (2 mg/mL), 10 mL Multiple Dose Vial packaged in a carton, Rx only, Teva Parenteral Medicines, Inc., Irvine, CA 92618, NDC 0703-4685-01.
by Teva North America
- Reason
- Failed Impurities/Degradation Specifications: High out of specification results for Impurity D.
- Published
- August 3, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Oxacillin for Injection, USP, 10 grams per pharmacy bulk package, Buffered - For IV Use, Sterile, Nonpyrogenic, Preservative-free, Rx Only, Mfd for Sagent Pharmaceuticals, Schaumberg, IL, 60196, USA, Made in India, NDC 25021-163-69
by Sagent Pharmaceuticals Inc
- Reason
- Presence of Particulate Matter; The firm received two product complaints for small, dark particulate matter identified in solution post reconstitution.
- Published
- August 3, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Divalproex Sodium Delayed-release Tablets USP, RX, 250 mg, 100 count bottles, Manufactured in Israel by: TEVA PHARMACEUTICALS IND. LTD. Jerusalem, 9777402, Israel, Manufactured for: TEVA PHARMACEUTICALS USA, INC. North Wales, PA 19454, NDC 0093-7440-01.
by Teva North America
- Reason
- Failed Tablet/Capsule Specifications
- Published
- August 3, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Dextroamphetamine Sulfate Extended-Release Capsules, 10 mg, 90- count bottles, Rx Only Manufactured by: Actavis Elizabeth LLC Elizabeth, NJ 07207 USA; Distributed by: Actavis Pharma, Inc Parsippany, NJ 07054 USA NDC 45963-304-09
by Actavis Inc
- Reason
- Failed Dissolution Specifications
- Published
- August 3, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
CRF Frozen Foods, LLC
- Product
- Organic Root Medley, brand Organic by Nature, frozen, net wt…
- Reason
- Organic Root Medley is recalled because it has the potential to be contaminated with Listeria monocytogenes.
- Published
- August 3, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Frito-Lay, Inc
- Product
- 20 count SunChips & Rold Gold Mix packaged as 20 single flex…
- Reason
- Potential to contain undeclared peanuts.
- Published
- August 3, 2016
- Distribution
- Nationwide
View recall →
Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions.
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