DrugJul 13, 2016
Hospira Magnesium Sulfate Inj., USP 50%, 10 g/20 mL (0.5 g/mL) recall — FDA D-1137-2016
Presence of Particulate Matter: Confirmed customer complaint for the presence of particulate matter.
Class IFDA: OngoingHospira Inc.
Monthly breakdown
2016 recalls by month
Select a month to review the recall records reported during that period.
December 2016251 records · 2 categoriesNovember 2016140 records · 2 categoriesOctober 2016469 records · 2 categoriesSeptember 2016304 records · 3 categoriesAugust 2016156 records · 3 categoriesJuly 2016295 records · 2 categoriesJune 2016155 records · 2 categoriesMay 2016210 records · 2 categoriesApril 2016193 records · 2 categoriesMarch 2016166 records · 2 categoriesFebruary 2016176 records · 2 categoriesJanuary 201693 records · 2 categories
2016 recalls — page 67
Records are ordered by the best available source date.
DrugJul 13, 2016
Bee Extremely Amazed Infinity Capsules, 500 mg, 30-count bottle recall — FDA D-1141-2016
Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn…
Class IFDA: TerminatedBee Extremely Amazed LLC
DrugJul 13, 2016
Bee Extremely Amazed La' Trim Plus Capsules, 350 mg, 60-count bottles recall — FDA D-1143-2016
Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn…
Class IFDA: TerminatedBee Extremely Amazed LLC
DrugJul 13, 2016
QuVa Pharma PHENYLephrine 1 mg/10 mL (100 mcg/mL) in 0.9% Sodium Chloride, 10 mL syringe recall — FDA D-1066-2016
Labeling: Label Error on Declared Strength. Product has correct label on the syringe and the case but some units are incorrectly labeled as .4 mg/10 mL (40 mcg/ml) on the light protective…
Class IFDA: TerminatedQuVa Pharma, Inc.
DrugJul 13, 2016
Bee Extremely Amazed SLIM TRIM U Capsules, 250mg, 60-count bottles recall — FDA D-1147-2016
Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn…
Class IFDA: TerminatedBee Extremely Amazed LLC
DrugJul 13, 2016
Bee Extremely Amazed Ultimate Formula Capsules, 250mg, 48-count bottles recall — FDA D-1148-2016
Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn…
Class IFDA: TerminatedBee Extremely Amazed LLC
DrugJul 13, 2016
Bee Extremely Amazed Oasis Capsules, 500mg, 45-count bottles recall — FDA D-1144-2016
Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn…
Class IFDA: TerminatedBee Extremely Amazed LLC
DrugJul 13, 2016
Lyne Laboratories Cyproheptadine Hydrochloride Syrup, Oral Solution USP, 2 mg/5 mL recall — FDA D-1062-2016
Subpotency: product assayed and found OOS for cyproheptadine
Class IIIFDA: TerminatedLyne Laboratories, Inc.
DrugJul 13, 2016
Bee Extremely Amazed Asset BOLD Capsules, 500 mg, 60-count bottles recall — FDA D-1138-2016
Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn…
Class IFDA: TerminatedBee Extremely Amazed LLC
DrugJul 13, 2016
Bee Extremely Amazed SlimeX-15 Capsules, 15 mg, 30-count bottles recall — FDA D-1146-2016
Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn…
Class IFDA: TerminatedBee Extremely Amazed LLC
FoodJul 6, 2016
Maytag Blue Cheese recall — FDA F-1595-2016
Product is contaminated with Listeria monocytogenes.
Class IFDA: TerminatedMaytag Dairy Farms Inc.
FoodJul 6, 2016
Jel Sert Co Margaritaville 4.16 ounce packages of Banana creme pie filling recall — FDA F-1594-2016
There was a positive salmonella sample from another customer of the supplier that tested it. This firm uses the freeze dried bananas in their Banana creme pie filling mix.
Class IFDA: TerminatedJel Sert Co.
FoodJul 6, 2016
Reser's Fine Foods, Inc. - Century Walmart Redskin Potato Salad, Refrigerated, Retail net wt recall — FDA F-1580-2016
Walmart Redskin Potato Salad is recalled due to a potential to be contaminated with Listeria monocytogenes. This product was made with one lot of onion which was recalled by supplier.
Class IFDA: TerminatedReser's Fine Foods, Inc. - Century
FoodJul 6, 2016
Reser's Fine Foods, Inc. - Century Safeway Classic Potato Salad, Refrigerated, Retail recall — FDA F-1578-2016
Safeway Classic Potato Salad is recalled due to a potential to be contaminated with Listeria monocytogenes. This product was made with one lot of onion which was recalled by supplier.
Class IFDA: TerminatedReser's Fine Foods, Inc. - Century
FoodJul 6, 2016
Pita Pal Mediterranean Three Bean Net Wt recall — FDA F-1583-2016
Product may be contaminated with Listeria monocytogenes.
Class IFDA: TerminatedPita Pal Foods LP
FoodJul 6, 2016
Pita Pal Texas Caviar Net Wt recall — FDA F-1584-2016
Product may be contaminated with Listeria monocytogenes.
Class IFDA: TerminatedPita Pal Foods LP
FoodJul 6, 2016
R. J. Van Drunen and Sons Freeze dried banana 1/4 diced packaged in 20 lb recall — FDA F-1593-2016
Customer received a 1,000g sample of freeze dried bananas, had it tested at 3rd party lab and received a positive test result for Salmonella.
Class IFDA: TerminatedR. J. Van Drunen and Sons Inc.
FoodJul 6, 2016
Reser's Fine Foods, Inc. - Century Safeway Tuna Salad, Refrigerated, Retail package, Net wt recall — FDA F-1579-2016
Safeway Tuna Salad is recalled due to a potential to be contaminated with Listeria monocytogenes. This product was made with one lot of onion which was recalled by supplier.
Class IFDA: TerminatedReser's Fine Foods, Inc. - Century
FoodJul 6, 2016
Reser's Fine Foods, Inc. - Century Refrigerated, Retail package, Net wt recall — FDA F-1575-2016
Potato Salad is recalled due to a potential to be contaminated with Listeria monocytogenes. This product was made with one lot of onion which was recalled by supplier.
Class IFDA: TerminatedReser's Fine Foods, Inc. - Century
FoodJul 6, 2016
Reser's Fine Foods, Inc. - Century Savemart Potato Salad, Refrigerated, Foodservice package recall — FDA F-1581-2016
Savemart Potato Salad is recalled due to a potential to be contaminated with Listeria monocytogenes. This product was made with one lot of onion which was recalled by supplier.
Class IFDA: TerminatedReser's Fine Foods, Inc. - Century
FoodJul 6, 2016
Reser's Fine Foods, Inc. - Century Refrigerated, Retail package, Net wt recall — FDA F-1574-2016
Deviled Egg Potato Salad is recalled due to a potential to be contaminated with Listeria monocytogenes. This product was made with one lot of onion which was recalled by supplier.
Class IFDA: TerminatedReser's Fine Foods, Inc. - Century
FoodJul 6, 2016
Reser's Fine Foods, Inc. - Century Stonemill Kitchens Classic Potato Salad, Refrigerated recall — FDA F-1577-2016
Stonemill Kitchens Classic Potato Salad is recalled due to a potential to be contaminated with Listeria monocytogenes. This product was made with one lot of onion which was recalled by…
Class IFDA: TerminatedReser's Fine Foods, Inc. - Century
FoodJul 6, 2016
Eban Bakery Gluten Free Breads and Baked Goods Product is labeled as "eban's BAKEHOUSE recall — FDA F-1591-2016
The firm did not list the allergen,"coconut" on the "Contains:" portion of the product label. Coconut is listed in the "Ingredients:" portion on the product label.
Class IIFDA: TerminatedEban Bakery Gluten Free Breads and Baked Goods LLC
FoodJul 6, 2016
Pita Pal Chipotle Quinoa & Black Beans Superfood Mild Net Wt recall — FDA F-1585-2016
Product may be contaminated with Listeria monocytogenes.
Class IFDA: TerminatedPita Pal Foods LP
About the 2016 recall archive
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.