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Abiomed is recalling 900 Impella heart pump controllers in three products: Automated Impella Controller, Impella Optical Controller, and Impella Connect Optical AIC. The units need hardware, firmware, or software updates found during a review of servicing records. Possible problems include the controller failing to recognize the purge cassette, a sticking push button that can cause loss of console control, start-up failure, and a software defect that can show incorrect negative pressure readings. No injuries have been reported.

Serious·FDA·Oct 28, 20263 products

JXK Enterprises, Inc. is voluntarily recalling Boner Bears Chocolate, Lot #BB21125, sold as a male enhancement product. FDA lab testing found sildenafil, the active ingredient in the prescription drug Viagra, which is not listed on the label. The product was sold nationwide online through www.elyxr.com.

Serious·FDA·Oct 28, 2026

GF Blends is recalling three gluten-free baking mixes because they may contain wheat gluten that is not listed on the label. The products are sold as Gluten Free Truly AIP flour, bread mix and the EAT G.A.N.G.S.T.E.R pizza crust and flat bread mix, and were sold nationwide online at eatgangster.com, trulyaip.com and Amazon.com. No injuries have been reported.

Serious·FDA·Oct 28, 20263 products

Haifa Smoked Fish of Queens, NY is recalling about 560 pounds of cold smoked sprats because they may be contaminated with Clostridium botulinum, the bacterium that causes botulism. The sprats were sold at retail stores in New Jersey, New York, and Pennsylvania. The company has reported no illnesses to date.

Serious·FDA·Oct 27, 2026·Haifa Smoked Fish

Oliva on Main is recalling three Riad's Oliva to Go products: Baba Ghanouj, Spicy Baba Ghanouj, and Hummus. The products contain sesame, which is not listed on the label. The recall covers products sold in Massachusetts and Connecticut.

Serious·FDA·Oct 27, 20263 products

Greenwich Rx is recalling 4,319 vials of its 200 mg/mL glutathione injection (10 mL multi-dose vials, for subcutaneous use only) because they may be contaminated with microbes. The recall covers 12 lots with beyond-use dates from October 2 to November 26, 2026, distributed nationwide. No injuries have been reported.

Serious·FDA·Oct 27, 2026·Greenwich Rx

Par Health USA's Argatroban Injection vials contain unwanted particles—including cellulose, polystyrene, plastic, stainless steel, or rubber stopper material—in the solution. The contamination affects multiple lot numbers distributed nationwide. No injuries have been reported.

Serious·FDA·Oct 26, 20262 products

Tonight We Ride, LLC recalled all lots of Ultimate Forza Male Supplement capsules because they contain three undeclared active ingredients: sildenafil and tadalafil (prescription drugs sold as Viagra and Cialis) and dapoxetine (not approved by the FDA). These ingredients were found through third-party testing and pose health risks, especially for people taking nitrate medications or with heart conditions.

Serious·FDA·Oct 24, 2026

Imperio Distribution LLC recalled approximately 946 pounds of ready-to-eat beef jerky products packaged between January and October 2026 because they were produced without federal inspection. The products also carried an unauthorized USDA inspection mark. These items were distributed to retailers in Illinois, Indiana, Iowa, Michigan, Minnesota, Missouri, and Wisconsin.

Serious·USDA·Oct 24, 2026·Imperio Fuego

Eden Brothers Broccoli Seeds (Calabrese variety) in 1 oz and 1 pound pouches may be contaminated with Salmonella. The affected product was packed in 2027 under lot numbers 1022067 and 1022068, and was distributed nationwide.

Serious·FDA·Oct 23, 2026

ZestiGreens Broccoli Seeds for Sprouting & Microgreens (8 oz and 16 oz packages) may be contaminated with Salmonella. The seeds were primarily sold through Amazon. No illnesses have been reported.

Serious·FDA·Oct 23, 2026

Natural Grocers Brand Organic 2-Pound Mung Beans may contain sharp glass fragments. The company received customer complaints about glass in the product and is recalling affected packages. No injuries have been reported so far.

Serious·FDA·Oct 22, 2026·Natural Grocers

EAK Distribution LLC is recalling Heirloom Homegrown Green Sprouting Calabrese Broccoli Sprout Seeds (8 oz packets) sold on Amazon due to potential Salmonella contamination. The affected lot is AUG172026, and approximately 3,600 packets were distributed nationwide.

Serious·FDA·Oct 22, 2026

Gardeners Basics brand Waltham 29 Broccoli Sprouting Seeds have been recalled due to potential Salmonella contamination. The affected product is packaged in a 1-pound white and green resealable pouch with UPC 848137042889 and marked "Packed for 2027". About 235 bags were distributed nationwide through online sales.

Serious·FDA·Oct 22, 2026

BAMAMON LED Projecting Finger Light toys contain button cell batteries that can be swallowed, posing a serious injury or death risk to young children. The toys, sold in 32-piece boxes with space-themed projections, violate federal safety standards for toys.

Serious·CPSC·Oct 22, 2026

Costway convertible high chairs lack a required safety restraint system, allowing children to slip through the gap between the feeding tray and seat. This can lead to entrapment or falls, creating a serious injury or death hazard.

Serious·CPSC·Oct 22, 2026

VQQQ-branded natural gas patio heaters (models VQQQ-A1 and VQQQ-001) can malfunction, causing gas to leak. This poses a risk of serious injury or death from fire and burns. About 100 units were sold online via Amazon between July 2024 and August 2026.

Serious·CPSC·Oct 22, 2026

CIYTI Light-Up Princess Costumes contain button cell batteries in the crown, scepter, and remote control that children can access easily. If swallowed, these batteries can cause serious internal injuries or death.

Serious·CPSC·Oct 22, 2026

Medtronic MiniMed CareLink Clinic software version 4.4A has a defect in its Settings Calculator feature. When healthcare providers enter custom insulin values, the calculator ignores them and continues using default values instead. This can result in incorrect insulin dose recommendations being sent to patients' insulin pumps, potentially causing patients to receive too much or too little insulin.

Serious·FDA·Oct 21, 2026

Medline distributed 165 open heart surgical convenience kits (SKU DYNJ902898D) with cannula components that don't meet required safety dimensions. The defective cannulas may leak or break during use, which could compromise patient safety during surgery.

Serious·FDA·Oct 21, 202612 products

Baxter Healthcare's Likorall overhead patient lifts may experience motor shaft breakage combined with reduced safety system performance, causing the lift strap to lower faster than expected during use. This malfunction could result in patient injury if a significant fall occurs.

Serious·FDA·Oct 21, 2026

The IOMAX Cortical Module, a medical device used for electrical stimulation testing, contains a defective printed circuit board that may cause the device to deliver electrical stimulation to a patient unintentionally or allow unwanted electrical current to reach the patient. The issue affects 23 devices with specific serial numbers distributed in the US and internationally.

Serious·FDA·Oct 21, 2026·Cadwell

Medtronic identified that donor tissue used in batch A62881 of Grafton DBM bone graft products tested positive for Clostridium butyricum bacteria and did not meet donor eligibility standards. Although the finished product passed sterility testing and underwent radiation treatment, there is a possibility of Clostridium infection if the product is implanted. Medtronic is retrieving all unused product from this batch.

Serious·FDA·Oct 21, 20262 products

Jenavalve Technology Inc. is recalling certain Trilogy Delivery Catheter devices (27MM, REF: TRILOGY-DC-L) because the sleeve liner may separate inside the catheter. This separation can make it difficult or impossible to properly deploy the heart valve device during surgery.

Serious·FDA·Oct 21, 2026·Jenavalve3 products

Instrumentation Laboratory is recalling two part numbers of the HemosIL AcuStar HIT-IgG(PF4) in vitro diagnostic test, 1,848 units in total. The test may produce an invalid calibration curve, or patient results may read up to 47% lower than they should. The recall covers US states and countries worldwide. No injuries have been reported.

Serious·FDA·Oct 21, 20262 products

Primal Herbs Volume, sold as a herbal supplement, contains sildenafil—a prescription medication—that is not listed on the label. FDA testing confirmed the presence of this undeclared ingredient. The product was sold online between July 2 and September 19, 2025.

Serious·FDA·Oct 21, 2026·Primal Supplements

Wild West Seed Inc is recalling specific lots of broccoli seeds (Green Sprouting Calabrese lot #4105 and Waltham29 lot #4475) because they may be contaminated with Salmonella. The seeds were distributed across multiple states and the United Kingdom.

Serious·FDA·Oct 21, 2026

Pacific Health Sciences' Babies' Magic Tea Baby Sleep Gripe Water contains elevated levels of alcohol, despite being labeled as alcohol-free. The product is marketed for infants as young as 2 weeks old. About 953 units with lot number 25122bw and expiration date 12/2028 were sold through Amazon and a customer website.

Serious·FDA·Oct 21, 2026

Deano's Pasta Pear and Pecorino Triangoli Ravioli contains undeclared lobster, which is not listed on the label. People with shellfish allergies could have a serious allergic reaction if they eat this product. The recall affects specific lot codes distributed in Massachusetts and New Hampshire.

Serious·FDA·Oct 21, 2026·Deano's Pasta

Par Health USA's Dexmedetomidine HCl injection vials contain unwanted particulate matter, identified as cellulose or stopper material. The contamination affects two specific lots distributed nationwide. This is a prescription medication used during anesthesia and sedation.

Serious·FDA·Oct 21, 2026