Summary Company Announcement Date: January 10, 2020 FDA Publish Date: January 10, 2020 Product Type: Drugs Reason for Announcement: Recall Reason Description Cross contamination with another drug substance, Enalapril Maleate Company Name: Taro Pharmaceuticals U.S.A., Inc. Brand Name: Brand Name(s) Taro Pharmaceuticals Product … [Read more...]
KME ( 20V006000 )
Dated: JAN 08, 2020 Kovatch Mobile Equipment Corp. (KME) is recalling one 2017 and certain 2012-2015 Emergency Response KME 55 FT Firestix Aerial Devices. The swing drives may not contain lubricating oil, which can cau... … [Read more...]
FSIS Issues Public Health Alert for Swedish Meatball Products Due to Misbranding and an Undeclared Allergen
WASHINGTON, Jan. 9, 2020 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert because Carso’s Pasta Company, a Lynnwood, Wash. establishment, sold 636 pounds of ready-to-eat (RTE) Swedish meatball products that were misbranded. The products contain anchovies (fish), which are not declared … [Read more...]
MICRO BIRD ( 20V005000 )
Dated: JAN 06, 2020 Corp. Micro Bird Inc. (Micro Bird) is recalling certain 2015-2019 T-Series school buses. The 150A circuit breaker located under the driver's seat may be oversized and may not open fast enough to powe... … [Read more...]
MICRO BIRD ( 20V004000 )
Dated: JAN 06, 2020 Corp. Micro Bird Inc. (Micro Bird) is recalling certain 2015-2019 CT-Series shuttle buses. The 150A breaker located under the driver's seat may be oversized and may not open fast enough to power off ... … [Read more...]
Libbey Glass Recalls Milk Bottles Due to Laceration Hazard
The bottles can break unexpectedly during use, posing a laceration hazard. … [Read more...]
Thesaurus Global Marketing Recalls Tricycles Due to Violation of the Federal Lead Paint Ban; Risk of Poisoning; Sold Exclusively at Amazon.com (Recall Alert)
Paint on the canopy’s frame contains levels of lead that exceed the federal lead paint ban and tricycle components contain levels of lead that exceed the federal lead content ban. Lead is toxic if ingested by young children and can cause adverse health issues. … [Read more...]
Boston Warehouse Trading Corp. Recalls Holiday Travel Mugs Due to Fire Hazard; Sold Exclusively at Meijer Stores
The mugs are mislabeled as microwave safe. If microwaved, the metallic print on the mug can spark, posing a fire hazard. … [Read more...]
Mavidon Issues Voluntary Worldwide Recall of Manufactured Products Including Lemonprep® Tubes And Single Use Cups Pediaprep® Tubes And Single Use Cups Wave Prep® Tubes And Single Use Cups Cardio Prep Single Use Cups Due To Burkholderia Cepacia Contamination
Summary Company Announcement Date: December 23, 2019 FDA Publish Date: January 08, 2020 Product Type: Medical Devices Reason for Announcement: Recall Reason Description Burkholderia cepacia Company Name: Mavidon Brand Name: Brand Name(s) LemonPrep®, PediaPrep®, Wave Prep, Cardio Prep Product Description: Product … [Read more...]
Denton Pharma, Inc. dba Northwind Pharmaceuticals Voluntarily Recalls All Unexpired Lots of its Ranitidine Tablets and Ceases Distribution, Due to Possible Presence of N-nitrosodimethylamine (NDMA) Impurity
Summary Company Announcement Date: January 06, 2020 FDA Publish Date: January 08, 2020 Product Type: Drugs Reason for Announcement: Recall Reason Description NDMA (Nitrosodimethylamine) impurity Company Name: Denton Pharma, Inc. dba Northwind Pharmaceuticals Brand Name: Brand Name(s) Product Description: Product Description Ranitidine … [Read more...]
Fresh Location Announces Product Recall Due to Possible Listeria Contamination
Summary Company Announcement Date: January 07, 2020 FDA Publish Date: January 08, 2020 Product Type: Food & BeveragesSnack Food ItemFoodborne Illness Reason for Announcement: Recall Reason Description Potential to be contaminated with Listeria monocytogenes Company Name: Fresh Location Brand Name: Brand Name(s) Fresh Location Product … [Read more...]
Mylan Initiates Voluntary Nationwide Recall of Three Lots of Nizatidine Capsules, USP, Due to the Detection of Trace Amounts of NDMA (N-Nitrosodimethylamine) Impurity Found in the Active Pharmaceutical Ingredient Manufactured by Solara Active Pharma Sciences Limited
Summary Company Announcement Date: January 08, 2020 FDA Publish Date: January 08, 2020 Product Type: Drugs Reason for Announcement: Recall Reason Description NDMA (Nitrosodimethylamine) impurity Company Name: Mylan N.V. Brand Name: Brand Name(s) Product Description: Product Description Nizatidine Capsules 150mg and 300mg Company … [Read more...]
SUBARU ( 20V002000 )
Dated: JAN 02, 2020 Subaru of America, Inc. (Subaru) is recalling certain 2009-2013 Forester, 2003-2006 Baja, 2004-2011 Impreza, 2004-2014 WRX (including STI), 2003-2014 Legacy and Outback, and 2006 Saab 9-2X vehicles or... … [Read more...]
SAAB ( 20V001000 )
Dated: JAN 02, 2020 Subaru of America, Inc. (Subaru) is recalling certain 2009-2013 Forester, 2003-2006 Baja, 2004-2011 Impreza, 2004-2014 WRX (STI included), 2003-2014 Legacy and Outback, and 2005-2006 Saab 9-2X vehicle... … [Read more...]
SUBARU ( 20V003000 )
Dated: JAN 02, 2020 Subaru of America, Inc. (Subaru) is recalling certain 2009-2013 Forester, 2003-2006 Baja, 2004-2011 Impreza, 2004-2014 WRX (including STI), 2003-2014 Legacy and Outback, and 2005-2006 Saab 9-2X vehicl... … [Read more...]
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