Connecticut recalls

Sold nationwide. AvKARE is recalling one lot of amitriptyline hydrochloride 10 mg tablets because they failed dissolution specifications. The recall covers 3,534 cartons of 50-count unit dose cards distributed nationwide. No injuries have been reported.

Moderate·FDA·Oct 28, 2026·AvKARE

Sold nationwide. Medtronic is recalling three CareLink SmartSync products, including the programmer, RF head patient connector and Device Manager app, because a software problem can cause an inaccurate displayed longevity estimate for implanted pulse generators. No injuries have been reported. The recall covers about 61,000 units distributed worldwide.

Moderate·FDA·Oct 27, 2026·Medtronic3 products

Sold nationwide. BioMerieux is recalling a limited number of EMAG nucleic acid sample preparation instruments used in clinical labs. After updating to firmware SP4 Patch 2, a random software error (Error 10003, Heater timeout) can cause delayed or no results when analyzing clinical samples. No injuries have been reported.

Moderate·FDA·Oct 27, 2026·bioMérieux

Sold nationwide. Philips is recalling 9 Azurion imaging system models, including Azurion 3, 5, 7 and S configurations. Some of these PCs may contain solid-state drives (SSDs) that are not specified in the Medical Device File, which could lead to reduced reliability over time, such as loss of imaging, a blank or black display, or trouble storing or accessing images. No injuries have been reported. The recall covers units distributed in the US and many other countries.

Moderate·FDA·Oct 27, 2026·Philips9 products

Sold nationwide. Canon Medical Systems is recalling 15 Alphenix interventional angiography X-ray systems (model INFX-8000C). A software issue can cause an internal error if F-Store or image acquisition is performed while the clinical analysis function is in use. The systems were distributed to hospitals and facilities in 18 states.

Moderate·FDA·Oct 27, 2026·Canon3 products

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, 2026·Oliva on Main3 products

Sold nationwide. Fei Fah Medical Manufacturing recalled its Ultra Strength Electric Medicated Balm because it did not meet FDA manufacturing quality standards (CGMP). The recall covers about 171,120 units sold nationwide in 70g and 10g sizes. No injuries have been reported.

Moderate·FDA·Oct 27, 2026·Fei Fah Medical Manufacturing

Sold nationwide. ABC Compounding Co. is recalling 19 antiseptic hand soap, antiseptic foam and hand-and-body wash products nationwide. The recall cites manufacturing practice violations (cGMP deviations), and no injuries have been reported. The products come from several makers and sellers, including ABC Compounding, and are sold under names such as Palm, Lynx, Aero Foamy, PRO CHEM and Chemseptic.

Moderate·FDA·Oct 27, 2026·ABC Compounding19 products

Sold nationwide. 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

Sold nationwide. Philips North America has recalled Model 712010 devices due to a potential for the device to fail immediately after exposure, which could cause the system to stop working. Approximately 563 units are affected.

Moderate·FDA·Oct 26, 2026·Philips

Sold nationwide. 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, 2026·Paragon 282 products

Sold nationwide. ValuHealth Extra Strength Pain Relief Acetaminophen 500 mg bottles have an incorrect label on the bottle itself. The outer carton correctly says "Acetaminophen 500 mg," but the label on the bottle says "Pain Relief PM" — a different product. This mismatch could cause confusion about what you're taking.

Moderate·FDA·Oct 26, 2026·Prodose

Sold nationwide. GSMS Incorporated is recalling 30-count packs of Carboxymethylcellulose Sodium 0.5% Lubricant Eye Drops (NDC 51407-945-30), made by Huons Co., Ltd. in South Korea. Testing detected polyethylene (PE)-related oligomers, so the product failed its impurities and degradation specification. No injuries have been reported.

Moderate·FDA·Oct 26, 2026·Huons

Sold nationwide. Strides Pharma is recalling one lot of Cinacalcet 30 mg tablets because they failed to meet dissolution specifications, meaning the tablets may not break down properly in the body. This could result in inconsistent or reduced drug effectiveness. The affected lot is 7717825A, expiring 11/30/2028.

Moderate·FDA·Oct 26, 2026·Strides

Sold nationwide. Macleods Pharma USA is recalling specific lots of Olmesartan Medoxomil, Amlodipine, and Hydrochlorothiazide combination tablets (40 mg/10 mg/12.5 mg) because they failed to meet dissolution specifications. This means the tablets may not break down properly in the body, potentially reducing how well the medication works.

Moderate·FDA·Oct 26, 2026·MacLeods Pharma

Sold nationwide. 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·Tonight We Ride

Sold nationwide. Certain Ziehm Orthoscan VERSA accessory carts and Versa Mini C-Arm systems have welds that do not meet specifications. This defect could cause the monitor arm mounting structure to separate from the cart during use.

Moderate·FDA·Oct 23, 2026·Ziehm Imaging

Sold nationwide. Medtronic has recalled certain OmniaSecure Model 3930M ventricular leads (used in heart devices for pacing and defibrillation) due to reports of difficulty achieving proper fixation during implantation. This implantation difficulty could potentially cause tissue trauma during the surgical procedure.

Moderate·FDA·Oct 23, 2026·Medtronic

Miyoko's Creamery European Style Salted Plant Milk Butter (8 oz units, UPC 857554005773) has been recalled because some packages may contain yeast, mold, and E. coli. The affected product was distributed to Connecticut, Florida, Georgia, Iowa, Illinois, Indiana, Maryland, New Jersey, New Hampshire, and Wisconsin.

Moderate·FDA·Oct 23, 2026·Miyoko's Creamery

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·EDEN BROTHERS

Sold nationwide. 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·ZestiGreens

Sold nationwide. Hikma Pharmaceuticals is recalling Abirtega (abiraterone acetate) 250 mg tablets due to failed weight uniformity specifications. Lot 3047 (expiring July 2027) does not meet quality standards. The issue was identified during quality testing; no injuries have been reported.

Moderate·FDA·Oct 23, 2026·Hikma Pharmaceuticals

Sold nationwide. Safecor Health is recalling specific batches of metoclopramide 5 mg tablets manufactured for Teva Pharmaceuticals due to co-mingled tablets in the bottles. Co-mingling means tablets from different batches or products may have been mixed together. The affected lot is 3116509 with an expiry date of 07/31/2027.

Moderate·FDA·Oct 23, 2026·Safecor Health

Sold nationwide. Glenmark Pharmaceuticals is recalling Abiraterone Acetate Tablets USP 500 mg in 60-count bottles due to a labeling defect. The affected lot (13250135, expiring 11/2027) was distributed nationwide. No injuries have been reported.

Moderate·FDA·Oct 23, 2026·Glenmark

Sold nationwide. Ritedose Pharmaceuticals recalled one lot of Formoterol Fumarate Inhalation Solution (20mcg/2mL) because it failed quality testing for impurities and degradation. The affected lot (25BL0, expiring 02/28/2027) was distributed nationwide. No injuries have been reported.

Moderate·FDA·Oct 23, 2026·Ritedose

Sold nationwide. Halyard ANTERIOR HIP PACK surgical kits (model SOAH31) contain a component that was not properly sterilized before packaging. The component was placed outside the sterile barrier and did not receive the required sterilization treatment. This affects 56 kits distributed in Arizona with lot number 1689215 and expiration date 11/06/2026.

Moderate·FDA·Oct 22, 2026·AVID Medical2 products

Sold nationwide. Medline is recalling 13 surgical drape and medical convenience kit products because the adhesive can be difficult to remove from patients and may leave residue on the skin. No injuries have been reported. The recall covers US nationwide distribution and several other countries.

Moderate·FDA·Oct 22, 2026·Medline13 products

Sold nationwide. The radiopaque (X-ray visible) material on the Xact mole marker can detach during use. When this happens, the loose material may create artifacts (unwanted marks or shadows) on mammography images, potentially affecting image quality and interpretation.

Moderate·FDA·Oct 22, 2026·Solstice

Sold nationwide. Medtronic is recalling two product groups in its InterStim system: InterStim SureScan MRI leads and InterStim percutaneous extensions. The recall covers 2 products in total. The company says the wrong lead or extension may have been selected, and an incompatible one may stop the system from working as intended. This could delay surgery or require surgical replacement of the product. No injuries have been reported.

Moderate·FDA·Oct 22, 2026·Medtronic2 products

Sold nationwide. A software bug in MiniMed Go version 1.2.1 broke the long-acting insulin dose reminder feature for users who had it enabled in earlier versions. When users updated the app, the reminder stopped working silently—without any alert to the user. This could cause users to miss or delay insulin doses, or accidentally take a double dose if they're unsure whether they already dosed.

Moderate·FDA·Oct 22, 2026·Medtronic