Food and Beverage Recalls
Dollar General Corporation recalls Clover Valley Instant coffee
Goodlettsville, Tennessee – August 11, 2025 –Dollar General Corporation is recalling three (3) lots of its eight (8) ounce Clover Valley® Instant Coffee due to the potential presence of glass.
8-Ounce Clover Valley® Instant Coffee
Package UPC: 876941004069
Lot: L-5163 / Best By 12/13/2026
Lot: L-5164 / Best by 12/13/2026
Lot: L-5165 / Best by 12/14/2026
Customers can find the lot and best by date information around the neck of the unit.
Clover Valley® Instant Coffee was sold and distributed between July 9-21, 2025 exclusively in Dollar General retail stores located in the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA,ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI ,WV, and WY.
Fromi USA recalls Brie Royal Faucon Brie Royal Faucon Cheese
Fromi USA Recalls Brie Royal Faucon 1kg Because of Possible Health Risk
FROMI USA of New York, NY is recalling 12 Cases of Brie Royal Faucon 1kg, because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The Brie Royal Faucon 1kg was distributed to Cheese Plate Park Slope LLC, located at 400 7th Avenue, 11215 Brooklyn NY. The recalled cheese was then cut and sold to customers from Cheese Plate Brooklyn - Park Slope LLC., and Cheese Plate Brooklyn : Carroll Gardens from 07/24/2025 through 08/13/2025.
Quesito El Establo recalls Quesito El Establo Spanish Cheese (Quesito Colombiano)
Quesito El Establo Recalls Spanish Cheese (Quesito Colombiano) Because of Possible Health Risk
Quesito El Establo of Salem, NH is recalling all Spanish Cheese (Quesito Colombiano) manufactured in their facility, due to the presence of rodent, rodent activity, and other insanitary conditions during the manufacturing and storage process.
There are numerous hazards associated with rodents including the potential presence of Salmonella. Use or consumption of affected products may present risk of illness due to the potential presence of Salmonella, an organism which can cause serious and sometimes fatal infections in infants, young children, frail or elderly people, pregnant persons, persons with pre- existent pathology (e.g., patients with cancer undergoing chemotherapy treatments, organ transplant recipient, etc.) and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.
Wegmans New York recalls Wegmans Cheeses
Rochester, N.Y. – Wegmans Food Markets, Inc. is recalling Wegmans Medium Camembert Soft Ripened Cheese, and various products containing this cheese, because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The affected products were sold in the cheese department at all Wegmans stores located in Connecticut, Delaware, Maryland, Massachusetts, New Jersey, New York, North Carolina, Pennsylvania, Virginia, and Washington, D.C.
Medical Device Recalls
Max Mobility, LLC. recalls Max Mobility/Permobil Speed Control Dial Component
Max Mobility/Permobil has voluntarily expanded its recall of the SpeedControl Dial, a wired control option for the SmartDrive MX2+ Power Assist Device, due to safety and performance concerns. This voluntary action applies to all SpeedControl Dials manufactured and distributed between the dates of April 25, 2022 to July 08, 2025.
Relation to Existing/Prior Recall:
A Class I recall (Z-1116-2025, Z-1117-2025), RES # 96086 was originally initiated on December 20, 2024 to address a material change with the printed circuit board assembly (PCBA) in SpeedControl Dials manufactured and distributed between the dates of August 17, 2023 and November 21, 2024. The recall was later expanded on March 28, 2025, and included all units manufactured and distributed from August 17, 2023 up to March 10, 2025. Max Mobility/Permobil received 781 complaints associated with PCBA design. Of these complaints, five (5) were for serious injuries, involving fractured or broken bones and a concussion. Information about prior recalls can be found using the links in the article.
This new expanded recall supersedes the previous recall and applies to all SpeedControl Dials in the market, including replacements received under the previous recall.
Tandem Diabetes Care, Inc. recalls Tandem Diabetes Care, Inc. t:slim X2 insulin pumps
Tandem Diabetes Care Issues Voluntary Medical Device Correction for Select t:slim X2 Insulin Pumps
SAN DIEGO – August 7, 2025 – Tandem Diabetes Care, Inc. (Nasdaq: TNDM) has announced a voluntary medical device correction for select t:slim X2 insulin pumps to address a potential speaker-related issue that can trigger an error resulting in a discontinuation of insulin delivery.
The error, which appears as a Malfunction 16 alarm to the user, will stop insulin delivery and terminate communication between the insulin pump and the continuous glucose monitoring (CGM) device. If not addressed, this could result in hyperglycemia due to discontinuation of insulin delivery, real-time CGM Estimated Glucose Values, and CGM trends. In severe cases of hyperglycemia, the user may require hospitalization or intervention from a medical professional. There have been 700 confirmed adverse events, defined as a confirmed high blood sugar and/or an event requiring medical intervention, and 59 reported injuries. No deaths have been reported.
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