Animal & Veterinary Recalls
Merck Animal Health Expands Voluntary Recall with Four Additional Lots of BANAMINE® / BANAMINE®-S (flunixin meglumine injection) in the U.S., Due to Presence of Particulate Matter
RAHWAY, N.J., Sept. 29, 2023 – Merck Animal Health, known as MSD Animal Health outside of the United States and Canada, a division of Merck & Co., Inc., Rahway, N.J., USA (NYSE:MRK), is voluntarily recalling four additional batches of BANAMINE® / BANAMINE®-S (flunixin meglumine injection) 50 mg/mL in the United States, used for injection in cattle, swine and horses due to the presence of particulate matter. These batches are in addition to the BANAMINE® / BANAMINE®-S recall of three batches dated Sept. 1, 2023 due to the presence of particulate matter. BANAMINE® / BANAMINE®-S (flunixin meglumine injection) is a prescription product in the U.S.
Drug Recalls
KVK-Tech, Inc. Issues Voluntary Nationwide Recall of One Lot of Betaxolol Tablets, USP 10 mg (Batch Number: 17853A) as a Precautionary Measure Due to a Single Foreign Tablet Found During the Line Clearance After the Batch was Packaged
FOR IMMEDIATE RELEASE – 09/29/2023 – Newtown, Pennsylvania, KVK-Tech, Inc. is voluntarily recalling one lot (Batch Number: 17853A; “the batch”) of Betaxolol Tablets, USP 10 mg, White, Round, film coated biconvex tablets, debossed “K” above bisect “13” on one side and plain on the other side” to the consumer level. The batch was distributed nationwide to wholesalers and retailers. The batch is being recalled as a precautionary measure due to a single Oxycodone HCl tablet 5 mg foreign tablet found on the packaging line during the line clearance after the subject batch was packaged. KVK has not received any reports of foreign tablet in any bottle of Betaxolol Tablets, USP 10 mg (Batch Number 17853A) at this time.
Hospira, Inc. Issues a Voluntary Nationwide Recall for 4.2% Sodium Bicarbonate Injection, USP and 1% and 2% Lidocaine HCl Injection, USP Due to the Potential for Presence of Glass Particulate Matter
FOR IMMEDIATE RELEASE - October 2, 2023 - NEW YORK, NY., Hospira, Inc., a Pfizer company, is voluntarily recalling the lots listed in the table below of 4.2% Sodium Bicarbonate Injection, USP, 5 mEq/10mL vial; 1% Lidocaine HCl Injection, USP, 50 mg/5mL vial; and 2% Lidocaine HCl Injection, USP, 100 mg/5mL vial to the user level. The recall was initiated due to the potential for presence of glass particulate matter.
There is an unlikely probability for serious adverse events, including death, should a patient receive an injectable product found to contain particulate matter identified as glass. Potential complications related to injection of visible and subvisible inert particles include inflammation of a vein, granuloma, and blockage of blood vessels or life-threatening blood clot events. The frequency and severity of these adverse events could vary depending upon a variety of factors including the size and number of particles in the drug product, patient comorbidities (such as age, compromised organ function), and presence or absence of vascular anomalies. The risk is reduced by the possibility of detection, as the label contains a clear statement directing the healthcare professional to visually inspect the product for particulate matter and discoloration prior to administration.
Biomic Sciences Issues Voluntary Nationwide Recall of ION* Sinus Support, ION* Biome Sinus, and Restore Sinus Spray Products Due to Microbial Contamination
FOR IMMEDIATE RELEASE – September 29, 2023 – Charlottesville, VA - Biomic Sciences is voluntarily recalling all lots of ION* Sinus Support, ION* Biome Sinus, and Restore Sinus Spray products to the consumer level. FDA testing found the product to contain microbial contamination identified as Microbacterium sp., Fictibacillus sp., Bacillus sp., (primarily B. malikii), and Paenibacillus sp (these microorganisms are generally non-pathogenic).
SCYNEXIS Issues a Voluntary Nationwide Recall of BREXAFEMME® (ibrexafungerp tablets) Due to Potential for Cross Contamination with a Non-Antibacterial ßlactam Drug Substance
JERSEY CITY, N.J., Sept. 27, 2023 (GLOBE NEWSWIRE) -- SCYNEXIS, Inc. is conducting a voluntary nationwide recall of 2 lots of BREXAFEMME® (ibrexafungerp tablets) to the consumer level in the US market due to potential cross contamination with a non- antibacterial ß-lactam drug substance in the ibrexafungerp citrate used to manufacture the BREXAFEMME® tablets. During a review of manufacturing equipment and cleaning activities at a supplier, SCYNEXIS was made aware of potential cross-contamination risk with a non-antibacterial beta-lactam drug substance. This press release provides additional details on the voluntary product recall recently disclosed by SCYNEXIS.
Food & Beverage Recalls
Cookies-N-Milk Issues Allergy Alert on Undeclared Peanuts in Chocolate Chip Edible Cookie Dough
Cookies-N-Milk, of McKinney, TX is recalling their 6oz cups of "Chocolate Chip Edible Cookie Dough" because it may contain undeclared peanuts. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products.
“Chocolate Chip Edible Cookie Dough” with lot # 32402342 C has been recalled which was made available in retail stores throughout the states of IA, KS, MN, MO, ND, NE, SD, WI, WY.
The recalled product is packaged in a 6oz clear plastic cup with the Cookies-N-Milk brand and the lot # 32402342 C found on the top side and is potentially filled with peanut butter edible cookie dough.
Orgain Issues Allergy Alert on Undeclared Sesame in Organic Plant Protein + Superfoods Powder, Creamy Chocolate Fudge Sold in Costco Warehouse Stores
Orgain LLC of Irvine, CA is voluntarily recalling a limited production run of its Organic Protein Powder + Superfoods, Creamy Chocolate Fudge flavor, because it may contain an undeclared sesame allergen.
People who have a sesame allergy or severe sensitivity to sesame run the risk of serious or life-threatening allergic reaction if they consume this product. Protein Powder + Superfoods, Creamy Chocolate Fudge 43.8 ounce/2.64 lb. is an item exclusively sold at Costco. The impacted product is limited to four lots and has been traced to select Costco warehouse locations, but not to Costco’s e-commerce site. No other Orgain products or retailers are affected by this voluntary recall.
Penzeys Spices Issues Allergy Alert on Undeclared Sesame Seeds in "Brady Street Cheese Sprinkle"
Penzeys Spices of Wauwatosa, WI, is voluntarily recalling some of its 2.2-ounce Jars of Brady Street Cheese Sprinkle (SKU/Item Number 20756) because they may contain undeclared sesame seeds. People who have allergies to sesame seeds run the risk of serious or life-threatening allergic reactions if they consume these products.
The Brady Street Cheese Sprinkle in question was distributed nationwide ONLY in Penzeys Retail Stores and through Internet or Phone orders beginning July 5, 2023.
The product comes in a 2.2-ounce, clear glass jar marked on the side with the following information:
- Batch/Lot # 37652-1 or 37652-2
- “BEST BY JUL 2024”
Eagle Produce LLC Recalls Whole Cantaloupe Because of Possible Health Risk
Eagle Produce LLC Scottsdale, AZ is initiating a voluntary recall of 6,456 cases of whole cantaloupe with the potential to be contaminated with Salmonella following a test conducted on cantaloupe in a distribution center by the FDA. Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy people may experience fever, nausea, vomiting, diarrhea (which may be bloody), and abdominal pain. In rare cases the organism can get into the bloodstream and producing more severe illness such as arterial infections (i.e. infected aneurysms), endocarditis and arthritis.
Dick Taylor Craft Chocolate Issues Recall for Allergy Allert on Undeclared Peanuts in “Ginger Snap Milk Chocolate”
Dick Taylor Craft Chocolate of Eureka, California is recalling “Ginger Snap Milk Chocolate” batch 23194 because they were mis-packaged and are Peanut Butter Dark Chocolate bars in Ginger Snap wrappers and contain undeclared peanuts. People who have allergies to peanuts are at risk of serious life-threatening allergic reaction if they consume these products.
The recalled “Ginger Snap Milk Chocolate” bars were distributed locally to retail accounts in Humboldt Couty, via online/mail orders and through our factory store in Eureka, California.
The product comes in a 2 oz wrapped chocolate bar marked with lot number 23194 on the back with an expiration date of 13/JAN/2025 stamped on the back. UPC 858788004495
TAMA Corporation Emite Un Alerta De Alergenos No Declarados: Trigo, Soya y Amarillo #5 En Las “Cachapas De Maiz Paisa”
Tama Corp. de Doral, FL, alerta que su producto "Cachapas de Maiz Paisa", en paquetes de 24 oz, contiene alergenos no declarados en la etiqueta: Trigo, Soya y Amarillo #5. Personas alérgicas a estos ingredientes corren el riesgo de reacciones alérgicas serias e incluso graves si consumen el producto.
Las "Cachapas de Maiz Paisa" fueron distribuidas a nivel nacional, en tiendas y supermercados.
El producto esta empacado en bolsas plásticas, transparentes.
. Los lotes afectados son: 31082301, 07092301, 06092301, 05092301, 04092301, 29082301, 30082301, 28082301, 31072301, 01082301, 02082301, 03082301, 08082301, 09082301, 10082301, 14082301, 15082301, 16082301, 17082301, 21082301, 22082301, 23082301, 24072301, 25072301, 26072301, 31072301, 28082301, 21072301, 27072301, 17082301, 14082301, 20072301, 21072301, 26072301, 07082301, 08062301, 30082301, 24082301, 12072301.
Read Comments