U.S. Recalls in June 2017

June 2017 recalls — page 2

These records include useful source details for the selected month.

2017 archive →

DrugJun 21, 2017

Pharmedium Services VANCOMYCIN HCl 1.5g in 300 mL 0.9% Sodium Chloride Injection USP recall — FDA D-0914-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Pharmedium Services Potassium PHOSphate added to 0.9% Sodium Chloride, 15 mMol 100 mL Bag recall — FDA D-0910-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Pharmedium Services Potassium PHOSphate in 0.5% Dextrose, 7.5 mMol in 100 mL, Service Code recall — FDA D-0908-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Pharmedium Services Potassium CHLORide added to 0.9% Sodium Chloride, 10mEq 100 mL Bag recall — FDA D-0907-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Pharmedium Services Potassium PHOSphate added to 0.9% Sodium Chloride, 10 mMol 100 mL Bag recall — FDA D-0911-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Pharmedium Services Potassium CHLORide added to 0.9% Sodium Chloride, 30mEq 100 mL Bag recall — FDA D-0906-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Bausch & Lomb NasalCrom (cromolyn sodium) Nasal Spray, USP, 5.2 mg per spray, 200 metered recall — FDA D-0899-2017

CGMP Deviations: Possibility of the presence of microbial contamination in the water used to manufacture this product lot.

Class IIFDA: TerminatedBausch & Lomb, Inc.

DrugJun 21, 2017

American Pharmaceutical Ingredients ESTRONE USP recall — FDA D-0919-2017

cGMP Deviations; lack of quality assurance.

Class IIFDA: TerminatedAmerican Pharmaceutical Ingredients LLC

DrugJun 21, 2017

Pharmedium Services VANCOMYCIN HCl 1.75g in 300 mL 0.9% Sodium Chloride Injection USP recall — FDA D-0915-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Pharmedium Services Potassium PHOSphate added to 0.9% Sodium Chloride, 7.5 mMol 100 mL Bag recall — FDA D-0909-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Pharmedium Services VANCOMYCIN HCl 1.5g in 300 mL 5% Dextrose Injection USP, Service Code recall — FDA D-0916-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Pharmedium Services Potassium PHOSphate added to 0.9% Sodium Chloride, 7 mMol 100 mL Bag recall — FDA D-0913-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIIFDA: TerminatedPharmedium Services, LLC

FoodJun 14, 2017

Alaska Pasta Company Riggatoni recall — FDA F-2353-2017

Undeclared soy lecithin. The firm used Canola oil cooking spray, which contains soy lecithin, in the manufacture of product but soy or soy lecithin is not declared on finished product label.

Class IIFDA: TerminatedAlaska Pasta Company

FoodJun 14, 2017

Alaska Pasta Company Ravioli Spinach recall — FDA F-2352-2017

Undeclared soy lecithin. The firm used Canola oil cooking spray, which contains soy lecithin, in the manufacture of product but soy or soy lecithin is not declared on finished product label.

Class IIFDA: TerminatedAlaska Pasta Company

FoodJun 14, 2017

STILL RIDING FOODS GLUTEN FREE PIZZA CRUST recall — FDA F-2335-2017

C. botulinum hazard in vacuum packaged pizza crust.

Class IIFDA: TerminatedStill Riding Foods, LLC

FoodJun 14, 2017

Alaska Pasta Company Gemelli recall — FDA F-2341-2017

Undeclared soy lecithin. The firm used Canola oil cooking spray, which contains soy lecithin, in the manufacture of product but soy or soy lecithin is not declared on finished product label.

Class IIFDA: TerminatedAlaska Pasta Company

FoodJun 14, 2017

Pinnacle Foods French toast packaged as follows: a) Hilltop HEARTH, FRENCH recall — FDA F-2310-2017

Potential for Listeria monocytogenes contamination

Class IIFDA: CompletedPinnacle Foods, LLC

FoodJun 14, 2017

Pinnacle Foods Homestyle pancakes packaged as follows: a) AUNT JEMIMA recall — FDA F-2299-2017

Potential for Listeria monocytogenes contamination

Class IIFDA: CompletedPinnacle Foods, LLC

FoodJun 14, 2017

Choice Northwest Love Your Heart Cake, Paradise Deli brand, Net Wt recall — FDA F-2328-2017

cake product is recalled due to undeclared soy lecithin. The canola spray oil containing soy lecithin was used but soy or soy lecithin is not declared on label.

Class IIFDA: TerminatedChoice Northwest

FoodJun 14, 2017

Alaska Pasta Company Spaghettoni recall — FDA F-2355-2017

Undeclared soy lecithin. The firm used Canola oil cooking spray, which contains soy lecithin, in the manufacture of product but soy or soy lecithin is not declared on finished product label.

Class IIFDA: TerminatedAlaska Pasta Company

FoodJun 14, 2017

Alaska Pasta Company Ravioli Mushroom recall — FDA F-2350-2017

Undeclared soy lecithin. The firm used Canola oil cooking spray, which contains soy lecithin, in the manufacture of product but soy or soy lecithin is not declared on finished product label.

Class IIFDA: TerminatedAlaska Pasta Company

FoodJun 14, 2017

Alaska Pasta Company Ravioli Lobster recall — FDA F-2349-2017

Undeclared soy lecithin. The firm used Canola oil cooking spray, which contains soy lecithin, in the manufacture of product but soy or soy lecithin is not declared on finished product label.

Class IIFDA: TerminatedAlaska Pasta Company

FoodJun 14, 2017

HEB Retail Support Center Hill Country Fare Thin Sandwich UPC 4122046090 recall — FDA F-2321-2017

Presence of rubber in the product.

Class IIFDA: TerminatedHEB Retail Support Center

FoodJun 14, 2017

Lamb Weston Red Robin Burgers and Brews Crispy Onion Rings, frozen, Net wt recall — FDA F-2337-2017

Red Robin Burgers and Brews Crispy Onion Rings, 14 oz. retail packages, are recalled due to undeclared milk.

Class IFDA: TerminatedLamb Weston Inc.

How to use this monthly recall archive

Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.

U.S. Recalls — June 2017

June 2017 recalls — page 2

How to use this monthly recall archive