AUGUST 19, 2021: Roche Diabetes Care issued a Medical Device Correction on ALL lots of the following Accu-Chek Aviva Plus and Accu-Chek Smartview test strips received in the past 18 months:

• Aviva Plus 10-count, 50-count (including 50-count mailorder) and 100-count
• Aviva Plus T/5 HLTH NWK NFRS 50-count
• Smartview 50-count (including 50-count mailorder) and 100-count

If you have one or ore of these products, please take the following actions:

BEFORE FIRST USE, check the vials of test strips and DO NOT USE if:

• The vial is open &/or damaged &/or the cap is damaged; &/or
• The cap is not fully closed &/or anything prevents it from closing properly.

If your product meets the above conditions, to get replacement test strips &/or if you have questions regarding this notification, please have your product available and contact Accu-Chek Customer Care using one of the following options:

1. Visit . Select "Support" then "Contact Us" to email or chat.
2. Call 1-866-805-5915 Monday-Friday from 8AM-8PM Eastern Standard Time

We apologize; no refunds can be issued by Kinney Drugs.

POSTED: 06/22/2021

Name: AKORN CONSUMER HEALTH

The manufacturer is pulling the product as a result of instability in the Vitamin A supplement within the product relating to products manufactured on and after August 2019.

POSTED: 05/28/2021

Name: THE LIBMAN COMPANY

The manufacturer is pulling the product due to potential swelling and leaking from the bottle.

IMPORTANT FYI - This product is safe to use.

The recall is based upon a missing paper insert in the box with instructions on opening the product cap.

VENDOR: Allergan USA Inc

SAFETY NOTICE

GSK Consumer Healthcare Requests that
Consumers Check Bottles for Holes in Five Excedrin Brands (Potential Failure to Meet Child Resistant Packaging Requirement)

HAZARD: If the bottle has a hole in the bottom that is large enough, children could access and swallow the contents, posing a potential safety risk.
PRODUCT: Certain lots of Excedrin Migraine Caplets, Excedrin Migraine Geltabs, Excedrin Extra Strength Caplets, Excedrin PM Headache Caplets, and Excedrin Tension Headache Caplets in large-sized bottles (50 count & above).
Please visit www.excedrin.com for a list of impacted lot #’s and additional information. Products currently available in stores are not impacted by this notice.
REMEDY: Consumers should examine their plastic bottles for holes, especially near the bottom. If such a condition is found, please contact GSK Consumer Healthcare:

1-800-468-7746
Monday – Friday, 8:00am – 6:00pm EST

This safety notice is being issued in cooperation with the
US Consumer Product Safety Commission (CPSC).

This recall has been issued due to a quality-related defect that does not meet vendor high-quality standards.

The specific recalled product information is listed below:

This recall has been issued due to the possibility of having holes in the 50, 80, 100, 125, 200, 250 and 300 count bottles supplied by the manufacturer.

The specific recalled product information is listed below:

PLANO, Texas – Aug. 24, 2020 – Frito-Lay today issued a voluntary recall of select 1 oz., 1 1/2 oz., 2 5/8 oz., 7 3/4 oz.,
12 1/2 oz., 15 1/2 oz. bags of Lay’s Barbecue Flavored Potato Chips because they may contain undeclared milk
ingredients. These recalled bags may also be included in select Frito-Lay Variety Packs. People who have an allergy or
severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction if they consume the product
contained inside the recalled bags.

The products covered by this recall were distributed in Arizona, California, Hawaii, Idaho, Montana, New Mexico,
Nevada, Oregon, Utah, Washington and Wyoming to retail stores and via foodservice, vending, e-commerce, mail
distribution and other channels.

No other Lay’s products, sizes, flavors, or variety packs are recalled.

The recall was initiated after it was discovered that bags of Lay’s Barbecue Flavored Potato Chips were inadvertently
filled with another flavor of potato chips, potentially exposing consumers to undeclared milk.

No allergic reactions related to this matter have been reported to date. Frito-Lay has informed the FDA of the action.

Consumers with the product noted above can return the product to a retailer for a refund or contact Frito-Lay Consumer Relations at 1-800-352-4477 (9 a.m. – 4:30 p.m. CST, Monday-Friday).

The specific recalled product information is listed below:

About Frito-Lay North America
Frito-Lay North America is the $17 billion convenient foods division of PepsiCo, Inc. (NASDAQ: PEP), which is
headquartered in Purchase, NY. Learn more about Frito-Lay at the corporate website, http://www.fritolay.com/ and
on Twitter http://www.twitter.com/fritolay.

About PepsiCo
PepsiCo products are enjoyed by consumers more than one billion times a day in more than 200 countries and
territories around the world. PepsiCo generated more than $67 billion in net revenue in 2019, driven by a
complementary food and beverage portfolio that includes Frito-Lay, Gatorade, Pepsi-Cola, Quaker and Tropicana.
PepsiCo's product portfolio includes a wide range of enjoyable foods and beverages, including 23 brands that
generate more than $1 billion each in estimated annual retail sales.

Consumer Instruction:  

voluntary recall is being issued on a limited number of KIND 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 product’s
label does mention that it “May contain sesame seeds.”

MANUFACTURER RECALL

If you have purchased the above product from Kinney Drugs, you may return to Kinney Drugs for a full refund.
 

Consumer Instruction:  

The RECALL is based on the appearance quality of the product:

MANUFACTURER RECALL

If you have purchased the above product from Kinney Drugs, you may return to Kinney Drugs for a full refund.
 

Only Products with the listed Best Before Date and listed LOT # are being Recalled

TheraFlu Cough - 6CT

The following item is being recalled due to a missing warning label on package.

If you have purchased the above product from Kinney Drugs, you may return to Kinney Drugs for a full refund. 

The company has received reports of product failures resulting in the release of the hot liquid from the Heat Gel-Core Insert component (orange ball) after being heated in the microwave.

Kinney Drugs has voluntarily removed Zantac OTC® & Premier Value® Acid Reducer products pending a U.S. Food and Drug Administration investigation of the ingredient ranitidine. Please ask your Kinney Pharmacist about alternative medications. 

The U.S. Food and Drug Administration has learned that some ranitidine medicines, including some products commonly known as the brand-name drug Zantac, contain a nitrosamine impurity called N-nitrosodimethylamine (NDMA) at low levels. NDMA is classified as a probable human carcinogen (a substance that could cause cancer) based on results from laboratory tests. NDMA is a known environmental contaminant and found in water and foods, including meats, dairy products, and vegetables.

The FDA has been investigating NDMA and other nitrosamine impurities in blood pressure and heart failure medicines called Angiotensin II Receptor Blockers (ARBs) since last year. In the case of ARBs, the FDA has recommended numerous recalls as it discovered unacceptable levels of nitrosamines.

The FDA is evaluating whether the low levels of NDMA in ranitidine pose a risk to patients. FDA will post that information when it is available. Patients should be able to trust that their medicines are as safe as they can be and that the benefits of taking them outweigh any risk to their health. Although NDMA may cause harm in large amounts, the levels the FDA is finding in ranitidine from preliminary tests barely exceed amounts you might expect to find in common foods.

Ranitidine is an over-the-counter (OTC) and prescription drug. Ranitidine is an H2 (histamine-2) blocker, which decreases the amount of acid created by the stomach. Over-the-counter ranitidine is approved to prevent and relieve heartburn associated with acid ingestion and sour stomach. Prescription ranitidine is approved for multiple indications, including treatment and prevention of ulcers of the stomach and intestines and treatment of gastroesophageal reflux disease.

The agency is working with international regulators and industry partners to determine the source of this impurity in ranitidine. The agency is examining levels of NDMA in ranitidine and evaluating any possible risk to patients. The FDA will take appropriate measures based on the results of the ongoing investigation. The agency will provide more information as it becomes available.

The FDA is not calling for individuals to stop taking ranitidine at this time; however, patients taking prescription ranitidine who wish to discontinue use should talk to their health care professional about other treatment options. People taking OTC ranitidine could consider using other OTC medicines approved for their condition. There are multiple drugs on the market that are approved for the same or similar uses as ranitidine.

Vendor Name: Cavallaro Foods
 
Item: Amy’s Kitchen Broccoli Cheddar Bake Bowl
 

Lot Codes affected is 60-D129
 
This recall is due to potential presence of foreign material.  Please check your shelves immediately and remove and dispose of any affected product.

TRP COMPANY

ALTAIRE PHARMACEUTICALS

PFIZER/WYETH - THERMACARE

Airborne Gummies

Frito-Lay: Stacy’s Simply Naked Pita Chips

Frito-Lay is preparing to initiate a limited voluntary recall of a very small number of 7 1/3 oz. bags of Stacy’s Simply Naked Pita Chips (more specifically described below) because they may contain undeclared milk ingredients. People who have an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction if they consume the product contained inside the recalled bags.

Kimberly-Clark:

EMERSON HEALTHCARE



MASON VITAMINS

PFIZER/WYETH THERMACARE

GLAXO SMITH KLINE

Valeant Pharmaceuticals

Cortaid

Emerson Healthcare

Premier Value Muscle Rub 4oz

Pepperidge Farm® Announces Voluntary Recall of Four Varieties of Goldfish® Crackers

ALVA-AMCO PHARMACAL CO.

Gravy Train Dog Food

J M Smucker Company is initiating a voluntary recall on selected wet dog food products. These products did not meet specifications because of a minor ingredient. This is not a threat to pet safety.

5 Hour ES Berry 6 Pack

The manufacturer, Living Essentails, has issued a voluntary recall due to possible defective packaging.

Hood Ice Cream Bars

The manufacturer of the product below has issued RECALL of the products below. The withdrawal is due to the possibility that the product may 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.

Nivea Cocoa Body Lotion

A voluntary recall has been issued by the manufacturer due to a quality issue.  Only the LOT # listed above is affected.

Bayer Asprin

This recall has been issued due to Stability Test results that did not meet specifications. If you have purchased the above product from Kinney Drugs, you may return to Kinney Drugs for a full refund.

Bush Baked Beans

PV Magnesium Citrate Oral low Sodium Lemon recall

This product has been recalled due to complaints of matter described as mold observed in product. The organism was identified as Rhinocladiella similis. 

EpiPen Recall

Please click on this link to access all the details from the manufacturer’s website. 

PV Powdered Medical Gloves

Baush & Lomb PeroxiClear

Frontier Natural Products - Aura Cacia Lavender Milk & Oat Bath

Entemann's Little Bites

Salmon Fish Strips Recall - ABO Gear LLC

Pharmavite Recall (Multiple Products) - June 7, 2016

Atkins Nutritionals - June 6, 2016

Atkins Nutritionals is voluntarily recalling the below due to the expansion of the SunOpta sunflower kernel recall for the potential presence of Listeria monocytogenes. Customer inquiries can be made by calling: 1-855-201-4611.

Consumer Instruction:

If you have purchased the above product from Kinney Drugs, you may return to Kinney Drugs for a full refund.

Hostess Brands - June 5, 2016

Hostess Brands has voluntarily recalled due to possible exposure to peanut allergens the below.

If you have purchased the above product from Kinney Drugs, you may return to Kinney Drugs for a full refund.Consumer Instruction: