FoodAug 29, 2018
Vidalia Valley glass jars 9oz UPC 0 42421 06956 3 & 64 oz UPC 0 42421 26517 0 recall — FDA F-1845-2018
The firm was notified that there is glass in the product.
Class IIFDA: TerminatedVidalia Valley, Inc.
Monthly breakdown
2018 recalls by month
Select a month to review the recall records reported during that period.
December 2018285 records · 4 categoriesNovember 2018342 records · 4 categoriesOctober 2018626 records · 4 categoriesSeptember 2018393 records · 4 categoriesAugust 2018569 records · 4 categoriesJuly 2018356 records · 4 categoriesJune 2018402 records · 4 categoriesMay 2018613 records · 4 categoriesApril 2018449 records · 3 categoriesMarch 2018523 records · 3 categoriesFebruary 2018612 records · 3 categoriesJanuary 2018290 records · 3 categories
2018 recalls — page 72
Records are ordered by the best available source date.
FoodAug 29, 2018
Pacific Coast Fruit Company Spinach Chopped 1", item # 73039 recall — FDA F-1851-2018
Product is recalled due to a potential contamination with Cyclospora.
Class IIFDA: TerminatedPacific Coast Fruit Company
FoodAug 29, 2018
Banks Square Market Corp dba The Produce Zuchini noodles packaged under the following brands recall — FDA F-1960-2018
Product may be contaminated with Listeria monocytogenes.
Class IIFDA: TerminatedBanks Square Market Corp dba The Produce Connection
FoodAug 29, 2018
SALT & STRAW Chocolate Gooey Brownie Ice Cream, packaged in pint-sized recall — FDA F-1846-2018
Chocolate Gooey Brownie Ice Cream is recalled due to possible undeclared peanuts.
Class IFDA: TerminatedSALT & STRAW LLC
FoodAug 29, 2018
Dole Fresh Vegetables 14 oz recall — FDA F-1833-2018
Recall of limited quantity of Classic Coleslaw due to potential for metal fragments in the product.
Class IIFDA: TerminatedDole Fresh Vegetables Inc.
FoodAug 29, 2018
Reser's Fine Foods item # 71117.15314, 2/4.5 # packages recall — FDA F-1849-2018
Bow Tie Florentine Reser's Fine Food is recalled due to a potential contamination with Cyclospora. The pasta salad contains spinach that was recalled due to a potential contamination with…
Class IIFDA: TerminatedReser's Fine Foods, Inc.
FoodAug 29, 2018
Reser's Fine Foods Bow Tie Pasta Caesar Molly's Kitchen, item # 58108.76434 recall — FDA F-1850-2018
Bow Tie Pasta Caesar Molly's Kitchen is recalled due to a potential contamination with Cyclospora. The pasta salad contains spinach that was recalled due to a potential contamination with…
Class IIFDA: TerminatedReser's Fine Foods, Inc.
FoodAug 29, 2018
Gift Services Inc Warehouse Sherman Candy Caramels are individually wrapped in plastic and recall — FDA F-1839-2018
Sherman Candy Caramels product is recalled due to undeclared pecans, walnuts, almonds and/or peanuts.
Class IFDA: TerminatedGift Services Inc Warehouse
FoodAug 29, 2018
Gourmet International SPARKLING MANDARIN JUICE DRINK, 6/34 oz., glass bottles recall — FDA F-1956-2018
Gourmet International Inc. is voluntarily recalling LItaly Sparkling Juice Beverages due to packaging concerns following multiple reports of leaking caps.
Class IIFDA: TerminatedGourmet International Inc.
FoodAug 29, 2018
Reser's Fine Foods Three Cheese Pasta Spinache Stonemill Kitchens, item # recall — FDA F-1848-2018
Three Cheese Pasta Spinache Stonemill Kitchens is recalled due to a potential contamination with Cyclospora. The pasta salad contains spinach that was recalled due to a potential…
Class IIFDA: TerminatedReser's Fine Foods, Inc.
FoodAug 29, 2018
J R Simplot Co Corporate HQ Simplot Good Grains Exotic Grains & Fire-Roasted Vegetable recall — FDA F-1844-2018
Simplot Good Grains Exotic Grains & Fire-Roasted Vegetable Blend is recalled due to undeclared wheat.
Class IIFDA: TerminatedJ R Simplot Co Corporate HQ
FoodAug 29, 2018
Graeters Manufacturing Company Graeter's HANDCRAFTED French Pot ICE CREAM, Limited Edition recall — FDA F-1837-2018
Product is labeled as gluten free, however, it contains wheat.
Class IIFDA: TerminatedGraeters Manufacturing Company
FoodAug 29, 2018
Natures Bounty BLUE GREEN ALGAE: Packaged under the following brands recall — FDA F-1835-2018
High level of microcystin observed in the product.
Class IIFDA: TerminatedNatures Bounty Inc.
FoodAug 29, 2018
Gourmet International SPARKLING POMEGRANETE JUICE DRNK, 6/34 oz., glass bottles recall — FDA F-1957-2018
Gourmet International Inc. is voluntarily recalling LItaly Sparkling Juice Beverages due to packaging concerns following multiple reports of leaking caps.
Class IIFDA: TerminatedGourmet International Inc.
DrugAug 29, 2018
VALSARTAN Camber Pharmaceuticals, Inc recall — FDA D-1114-2018
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Class IIFDA: CompletedHetero Labs Limited Unit V
DrugAug 29, 2018
Westminster Pharmaceuticals Levothyroxine and Liothyronine (Thyroid Tablets, USP), 1/2 grain recall — FDA D-1180-2018
Failed Content Uniformity Specifications: Product was manufactured using an adulterated active pharmaceutical ingredient; additionally, lack of process controls and good manufacturing…
Class IFDA: TerminatedWestminster Pharmaceuticals LLC
DrugAug 29, 2018
VALSARTAN Camber Pharmaceuticals, Inc recall — FDA D-1115-2018
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Class IIFDA: CompletedHetero Labs Limited Unit V
DrugAug 29, 2018
Westminster Pharmaceuticals Levothyroxine and Liothyronine (Thyroid Tablets, USP), 1/4 grain recall — FDA D-1181-2018
Failed Content Uniformity Specifications: Product was manufactured using an adulterated active pharmaceutical ingredient; additionally, lack of process controls and good manufacturing…
Class IFDA: TerminatedWestminster Pharmaceuticals LLC
DrugAug 29, 2018
VALSARTAN Camber Pharmaceuticals, Inc recall — FDA D-1113-2018
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Class IIFDA: CompletedHetero Labs Limited Unit V
DrugAug 29, 2018
Jubilant Cadista Pharmaceuticals Valsartan Tablets USP, 160 mg, 90-count bottle recall — FDA D-1105-2018
Incorrect/Undeclared Excipient: There is a potential an incorrect grade of excipient was used during manufacturing.
Class IIIFDA: TerminatedJubilant Cadista Pharmaceuticals, Inc.
DrugAug 29, 2018
Preferred Pharmaceuticals Valsartan Tablets USP 320 mg, 90-count, plastic child resistant recall — FDA D-1107-2018
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Class IIFDA: TerminatedPreferred Pharmaceuticals, Inc.
DrugAug 29, 2018
Jubilant Cadista Pharmaceuticals Valsartan Tablets USP, 80 mg, 90-count bottle recall — FDA D-1104-2018
Incorrect/Undeclared Excipient: There is a potential an incorrect grade of excipient was used during manufacturing.
Class IIIFDA: TerminatedJubilant Cadista Pharmaceuticals, Inc.
DrugAug 29, 2018
A-S Medication Solutions LLC Valsartan and Hydrochlorothiazide Tablets, Valsartan 160 MG and recall — FDA D-1110-2018
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Class IIFDA: OngoingA-S Medication Solutions LLC.
DrugAug 29, 2018
VALSARTAN Camber Pharmaceuticals, Inc recall — FDA D-1116-2018
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Class IIFDA: CompletedHetero Labs Limited Unit V
About the 2018 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.