Flagstone Foods, LLC. Issues Voluntary Recall of Wegmans Pecan Blend Due to Undeclared Almonds and Walnuts

/in /by
Flagstone Foods LLC, of Robersonville, NC, is recalling its 16-ounce packages of Wegmans Pecan Blend Trail Mix because they may contain undeclared almonds and walnuts. The product comes in a 16-ounce, plastic stand-up resealable package, marked with UPC Code 0-77890-31040-3 and lot code #05M04300 on

Source: Food and Drugs Administration--Recalls/Safety Alerts

4e Brands North America Issues Nationwide Voluntary Recall of Hand Sanitizer Due to Potential Presence of Undeclared Methanol (Wood Alcohol)

/in /by
4e Brands North America is voluntarily recalling ten (10) bottle sizes of Hand Sanitizers to the consumer level. The products are being recalled due to the potential presence of methanol (wood alcohol)

Source: Food and Drugs Administration--Recalls/Safety Alerts

Ridley Block Operations Voluntarily Recalls Ultralyx® 12% Protein Sheep

/in /by
Ridley Block Operations is voluntarily recalling Ultralyx® 12% Protein Sheep with batch number HB01679401. The product has been found to contain elevated levels of copper. With prolonged consumption, the affected product could potentially have adverse health effects on sheep, including reductions in

Source: Food and Drugs Administration--Recalls/Safety Alerts

Sundial Herbal Products is Recalling Products Attached Because these Products were Misbranded. The Products are Currently Unapproved Drugs, Recall is Required by the Order

/in , /by
To be in compliance with FDA Drug Regulations, Sundial is requesting an immediate recall, removal and return, of all Sundial Products, distributed from the period beginning January 1, 2014 through current, that have labeling containing/making drug claims stating the product(s) can diagnose, cure, mi

Source: FDA Food Safety Recalls RSS Feed

Maquiladora Miniara S.A. de C.V. Issues Voluntary Nationwide Recall of Shine and Clean Hand Sanitizer and Due to Potential Presence of Undeclared Methanol (Wood Alcohol)

/in /by
Maquiladora Miniara S.A. de C.V. is voluntarily recalling lots of Shine and Clean Hand Sanitizer gel to the consumer level. The products are being recalled due to the potential presence of methanol (wood alcohol) Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision,

Source: Food and Drugs Administration--Recalls/Safety Alerts

Lupin Pharmaceuticals, Inc. Issues Voluntarily Nationwide Recall of Metformin Hydrochloride Extended-Release Tablets, 500mg and 1000mg Due to the Detection of N-Nitrosodimethylamine (NDMA) Impurity

/in /by
Lupin Pharmaceuticals Inc. is voluntarily recalling all batches of Metformin Hydrochloride Extended-Release Tablets USP, 500mg and 1000mg to the consumer level. As part of the ongoing assessment and continuation of the dialog with the FDA, additional analysis revealed that certain tested batches wer

Source: Food and Drugs Administration--Recalls/Safety Alerts

Allergy Alert: KIND Issues Voluntary Recall Due to Undeclared Sesame Seeds in Oats & Honey

/in /by
KIND Healthy Snacks (KIND) is voluntarily recalling a limited number of Oats & Honey Granola with Toasted Coconut pouches due to the presence of sesame seeds, which is not listed as an ingredient in the product. The label does list “sesame seeds” under the “May Contain” statement.

Source: Food and Drugs Administration--Recalls/Safety Alerts

Mylan Initiates Voluntary Nationwide Recall of One Lot of Daptomycin for Injection, Due to The Presence of Particulate

/in /by
Mylan N.V. (NASDAQ: MYL) today announced that its U.S.-based Mylan Institutional LLC business is conducting a voluntary nationwide recall to the consumer level of one lot of Daptomycin for Injection, 500 mg/vial due to the presence of particulate matter found in one single-dose vial manufactured b

Source: Food and Drugs Administration--Recalls/Safety Alerts

ITECH 361 Issues Voluntary Nationwide Recall of All Clean Hand Sanitizer and Moisturizer and Disinfectant Due to The Potential Presence of Undeclared Methanol (Wood Alcohol)

/in /by
ITECH 361 is voluntarily recalling 18,940 bottles of All Clean Hand Sanitizer, Moisturizer and Disinfectant sold in one liter bottles to the consumer level. The products are being recalled due to the potential presence of methanol (wood alcohol).

Source: Food and Drugs Administration--Recalls/Safety Alerts

CME America Announces a Follow-Up on the Voluntary Recall of BodyGuard® Infusion System Administration Sets

/in /by
As part of CME America's commitment to quality, following the previously announced recall (April 27, 2020) of the BodyGuard® Infusion Pump Systems, the company conducted additional flow-rate accuracy testing. This testing revealed that some infusion sets do not meet the ±5% delivery accuracy for the

Source: Food and Drugs Administration--Recalls/Safety Alerts