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Recall Roundup: Ice cream improperly labeled; fentanyl patches contain different dose than labeled | Live Well CV: Health and Wellness

Recall Roundup: Ice cream improperly labeled; fentanyl patches contain different dose than labeled | Live Well CV: Health and Wellness

Recall Roundup: Ice cream improperly labeled; fentanyl patches contain different dose than labeled | Live Well CV: Health and Wellness

Among the products recalled last week are frozen tuna that may have been distributed to restaurants in the region, improperly labeled ice cream and fentanyl patches that don’t contain the right amount of fentanyl.

The U.S. Food and Drug Administration last week announced that Weis Markets issued a recall for its brand of Banana Puddin’ Ice Cream in 48-ounce containers because the product’s ingredient label fails to list an egg allergen. The product is safe to eat for those without egg allergies.

The product was sold in Pennsylvania and was packaged in a container with a UPC of 041497-01305. Customers who have purchased the product can return it for a full refund.

In other food news, the FDA also announced last week that Jensen Tuna of Louisiana is recalling its frozen ground tuna that was imported from JK Fish because it may contain salmonella.

The product was only sold as a wholesale case with 20 individual, one-pound bags in each case, and the product was sold to wholesalers in New York, as well as other states across the country. Those wholesalers then distributed the product to restaurants and retail locations, the FDA said.

The FDA urges restaurants and retailers to check their suppliers and not sell or serve recalled frozen ground tuna. Consumers with concerns should ask their restaurants and retailers whether the tuna dish they are purchasing contained the recalled tuna.

The FDA said the recall is in a response to its investigation into 13 illnesses caused by salmonella.

The FDA also announced the recall of fentanyl patches from Alvogen Inc. The company is recalling two lots of Fentanyl Transdermal System 12 mcg/h transdermal patches because they could contain 50 mcg/h of fentanyl instead.

The FDA said application of 50 mcg/h patch instead of the prescribed 12 could result in serious, life threatening or fatal respiratory depression. To date, the company has not received any reports of adverse events related to the issue, the FDA said.

The mislabeled products were distributed nationwide to the pharmacy level, and have expiration dates of May 2020 and June 2020.

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