FDA Warning & Recall Information

According to the FDA, Zyno Medical issued a Class I recall on several of their infusion pumps after discovery of a potentially dangerous software malfunction. The company announced the recall on September 13th, 2024, notifying all users via an Urgent Medical Device Correction letter. The […]

Late last week, Youngstown Grape Distributors Inc. issued a voluntary recall of two lots of their Happy Moose Juice, citing a production error and an increased risk of bacterial contamination. The recall was initiated on October 4th, and the FDA shared the company’s announcement on […]

Philips Respironics, Inc. has issued an Urgent Medical Device Correction for their series of Trilogy Evo ventilators due to concerns of aerosol deposits on the flow sensor when using in-line nebulizers. According to the FDA, the correction involves a field safety notice with updated guidelines […]

The Wisconsin-based company Jack and the Green Sprouts, Inc., is recalling two lots of its Alfalfa and Alfalfa Onion sprouts due to possible contamination with Listeria monocytogenes. According to the FDA, the company announced the recall on October 4th. The recalled products are sold in […]

As reported by the FDA, Mercury Medical has issued a Class I recall of their Neo-Tee T-Piece Resuscitators due to a potential malfunction with the inline controller. The company warns that continued use of the product could cause serious injury up to and including death. […]

The FDA recently notified the public of Lunds & Byerlys recall of two lots of their L&B Lone Star Dip after detection of mold in the product. The company announced the recall on Friday, October 4th. The impacted product has a UPC of 18169-74197 and […]

In conjunction with the FDA, Sentec/Percussionaire has announced a Class 1 correction to the usage instructions for the Phasitron 5 In-Line Valve, which is used for Intrapulmonary Percussive Ventilation (IPV). The company released the corrections after receiving six reports of injury from patients using recalled […]

According to the FDA, the Puerto Rican company Avole Inc. (Productos Nita) is recalling at least one lot of their Bacalaitos Criollos Codfish Frying Mix due to the omission of “pollock” (fish) from the list of ingredients. For those with an allergy or sensitivity, consumption […]

The FDA recently warned the public about a correction issued by Smiths Medical for its paraPAC Plus P300 and P310 Ventilators. The company requests that health care facilities follow all of the steps outlined in the correction recall to prevent injury and death while using […]

The FDA recently notified the public of the recall initiated by Grace Imports, LLC., of three lots of snack mixes after determining the product may contain undeclared wheat. At the end of August, a supplier notified the company that the asafetida, which is an herb […]

The FDA is reporting a recall initiated by Lystn, LLC., known on the market as ANSWERS, of four lots of dog food due to potential contamination with Salmonella and Listeria. The recall applies to specific lots of the company’s beef and chicken dog foods. ANSWERS […]

According to the FDA, Freesius Kabi is recalling one lot of the Ivenix LVP Primary Administration Sets Dual-Inlet, Low-Sorbing, Needle-Free Port, Y-Site due to a serious manufacturing defect. Continued use of the product could result in injury or death. Freesius Kabi sent the recall letter […]