Hawaii recalls

Sold nationwide. The 3mensio Workstation software may report heart and vessel measurements that are 0.8% to 34% larger than the actual size when specific conditions are met: the software is used with access only to 3D Echo or Mitral 3D Echo features, and the analysis involves Philips 3D echo datasets that contain Color Doppler data. This could lead to incorrect clinical measurements used in patient care decisions.

Moderate·FDA·Jul 29, 2026·PIE Medical Imaging

Sold nationwide. Certain Halyard EYE PACK convenience kits (Model LVEY27) contain Betadine solution at an incorrect concentration. The kits were distributed nationwide, primarily in California. No injuries have been reported.

Moderate·FDA·Jul 29, 2026·AVID Medical

Sold nationwide. SeaSpine Orthopedics has recalled certain Polyaxial Head spinal implants (REF 41-3010) due to a manufacturing error that may cause the polyaxial head to detach from the screw during surgery after insertion. This could require additional surgical intervention. The recall affects 796 units distributed worldwide, including nationwide US distribution and locations in Chile and Australia.

Moderate·FDA·Jul 29, 2026·SeaSpine

Sold nationwide. Olympus has identified a potential fault in the HDMI and DisplayPort connectors on certain OEV321UH 4K UHD LCD Monitors. This fault can result in image loss or display abnormalities. The recall affects 10 units with specific serial numbers distributed in Ohio, California, New Jersey, Florida, and Japan.

Moderate·FDA·Jul 29, 2026·Olympus

Sold nationwide. The roller assembly on the Ferno-Washington Power F2 Powered Fastening System may wear unevenly and deform, causing the rail mechanism to jam. If this happens, the stretcher cannot move along the rail—either with the powered system or manually—potentially delaying patient transport to a hospital.

Moderate·FDA·Jul 29, 2026·Ferno

Sold nationwide. ICU Medical's Hotline Fluid Warming Set (model L-70), a single-use device used to warm blood and IV fluids before delivery to patients, may leak due to inadequate solvent application at the tubing-to-connector bond in certain production lots. This defect could affect proper fluid delivery during patient care.

Moderate·FDA·Jul 29, 2026·ICU Medical

Sold nationwide. Paragon 28 received two complaints about breaches in the sterile barrier packaging of specific lots of the Phantom Hindfoot TTC/TC Ball Tipped Guide Rod (0.30 mm, 800 mm). The packaging breach could potentially allow contamination of the surgical device before use. No injuries have been reported.

Moderate·FDA·Jul 29, 2026·Paragon 28

Sold nationwide. Boston Scientific found that some air leak complaints were linked to damage to the sheath's hemostatic valve. The damage can happen when the dilator is inserted at the wrong angle during setup, and it may allow air into the device, creating a potential air embolism. This recall covers four FARADRIVE steerable sheath versions, with about 776,000 units affected. No injuries have been reported.

Moderate·FDA·Jul 29, 2026·Boston Scientific4 products

Sold nationwide. Boston Scientific identified specific FARASTAR Pulsed Field Ablation (PFA) generators with a configuration that cannot work safely with the FARAPOINT PFA catheter. Six units with specific serial numbers were distributed across Europe and need to be replaced.

Moderate·FDA·Jul 29, 2026·Boston Scientific

Sold nationwide. Boston Scientific is recalling three FARASTAR pulsed field ablation generator products because the instructions for use shipped with them did not include information about the FARAPOINT PFA catheter. A total of 30 units were affected, distributed in Austria, Spain, France, Germany, Denmark, Italy, Portugal, Great Britain, and Ireland. No injuries have been reported.

Moderate·FDA·Jul 29, 2026·Boston Scientific3 products

Sold nationwide. Medline Industries is recalling specific surgical convenience kits used in joint replacement procedures because they contain a pain-reliever medication (Bupivacaine Hydrochloride in Dextrose) with quality problems. The medication was manufactured by Huons Co, Ltd. and distributed through B. Braun Medical. The quality issues were identified by the supplier and no injuries have been reported.

Serious·FDA·Jul 29, 2026·Medline3 products

Sold nationwide. Wilcox Industries has released a software enhancement designed to increase the safety of its BOSS Xe aiming devices. The company is notifying all customers who purchased these products that the update should be installed.

Moderate·FDA·Jul 29, 2026·Wilcox Industries

Sold nationwide. TNVitamins 100% Organic Moringa Capsules (1,200 mg) and Moringa Powder (96 grams) have been found to be contaminated with Salmonella. The contamination affects specific lot numbers: Capsules (Lot #2800, expires 2/2028) and Powder (Lot #2782, expires 5/2028). No illnesses have been reported to date.

Serious·FDA·Jul 29, 2026·TNVitamins

Sold nationwide. Green Jeeva LLC's organic moringa powder (product code GJ96, lot 25/08001) tested positive for Salmonella. The powder was distributed in bulk to ingredient processors and distributors. No injuries have been reported.

Serious·FDA·Jul 29, 2026·Green Jeeva

Sold nationwide. Modern Warrior Ready, a dietary supplement sold in 60-capsule bottles, contains unapproved ingredients including tianeptine, 1,4 DMAA, and aniracetam. The FDA identified these ingredients through analysis. The product was distributed nationwide from April 2022 through December 8, 2025.

Serious·FDA·Jul 29, 2026·Modern Warrior

Sold nationwide. Fresenius Kabi is recalling five injectable medicine products because hair was found in some vials. The products are Xylocaine (two sizes), Naropin, lidocaine HCl injection and glycopyrrolate injection, all made by Fresenius Kabi in Lake Zurich, Illinois, and sold nationwide. No injuries have been reported.

Moderate·FDA·Jul 29, 2026·Fresenius Kabi5 products

Sold nationwide. Rising Pharma's Cyproheptadine Hydrochloride Syrup (2 mg/5 mL, 473 mL bottles) is being recalled because the medication is crystallizing and forming particles that float in the bottle. This affects specific batches distributed nationwide. No injuries have been reported.

Moderate·FDA·Jul 29, 2026·Rising Pharma

Sold nationwide. Rohto-Mentholatum is recalling eight Rohto Cooling Eye Drops products because they lack assurance of sterility, meaning the drops may not be guaranteed free of microbial contamination. All eight are sold under the Rohto Cooling Eye Drops name: ALL-IN-ONE, Max Strength (three versions), Optic Glow, Digi Eye, Dry Aid (single and twin pack), and Cool Relief. No injuries have been reported.

Moderate·FDA·Jul 29, 2026·Rohto-Mentholatum8 products

Sold nationwide. Ascend Laboratories is recalling one lot of amlodipine and olmesartan medoxomil combination tablets (10 mg/20 mg) because the olmesartan medoxomil active ingredient is below the required amount. This means affected tablets may not work as intended to lower blood pressure.

Moderate·FDA·Jul 29, 2026·Ascend Laboratories

Sold nationwide. Major Pharmaceuticals is recalling one lot of Levothyroxine Sodium Tablets, USP, 25 mcg due to subpotency — meaning the tablets contain less active ingredient than labeled. This affects Lot N02212 with an expiration date of 07/2026. Patients taking subpotent levothyroxine may not receive the full intended dose of this thyroid hormone replacement medication.

Moderate·FDA·Jul 29, 2026·Major Pharmaceuticals12 products

Sold nationwide. Precision Dose Inc. is recalling one lot of Glycopyrrolate Oral Solution (1 mg/5 mL) due to an unidentified impurity found during routine stability testing that does not meet specification. The affected lot (506033) expires November 30, 2026. This medication is prescription-only and supplied in unit-dose oral syringes.

Moderate·FDA·Jul 29, 2026·Precision Dose

Sold nationwide. Rooted in Rare brand Aquafaba Powder may contain undeclared egg, posing a serious allergic reaction risk for people with egg allergies or sensitivities. The recall affects 4 oz and 12 oz packages distributed through Amazon and the company website between June 2025 and July 2026.

Moderate·FDA·Jul 29, 2026·529 Commerce

Sold nationwide. Sunny Pharmtech is recalling three lots of Cyclophosphamide for Injection (1g and 2g vials) distributed between May 2024 and October 2024 because steel particles were found in the product. No injuries have been reported so far, but steel particles in an intravenous injection could cause serious complications including blood clots and infection.

Serious·FDA·Jul 24, 2026·Sunny Pharmtech

Sold nationwide. Baxter is recalling one lot of Cefazolin in Dextrose Injection (a frozen antibiotic infusion bag) because cardboard particles were found in the solution. The affected lot (LD175708, expiring February 14, 2027) was distributed between March and June 2025. No injuries have been reported so far.

Serious·FDA·Jul 24, 2026·Baxter

Sold nationwide. American Regent identified glass and paraformaldehyde particles in one lot of Papaverine Hydrochloride Injection (Lot #25202), a prescription medication used to improve blood circulation and treat muscle spasms. The particles could cause local irritation, blood vessel blockage, and serious complications including stroke.

Serious·FDA·Jul 24, 2026·American Regent

Sold nationwide. Snaps on Peony Design personalized baby bibs and stroller bags can detach, creating a choking hazard for young children. The bibs feature scalloped edges and personalized embroidery, while stroller bags have two snap-closure straps. About 52 items were sold online through Etsy between October 2025 and July 2026.

Serious·CPSC·Jul 23, 2026·Peony Design

Sold nationwide. CuddleCubs Creations teething toy sets sold on Amazon contain pull-string toys with silicone strings that are longer and smaller than safety standards allow. These strings can reach the back of a child's throat and become lodged, creating a serious choking hazard.

Serious·CPSC·Jul 23, 2026·YouRfocus

Sold nationwide. OeyUoc white pool drain covers sold on Amazon do not meet federal safety standards for drain protection and pose a serious risk of entrapment and drowning. The covers violate the Virginia Graeme Baker Pool and Spa Safety Act, which requires drain covers to prevent people—especially children—from getting trapped.

Serious·CPSC·Jul 23, 2026·Yuanxinxiang

Sold nationwide. Sviyatp white pool drain covers do not meet federal safety standards and pose a risk of entrapment and drowning. The covers were sold online as replacement drain covers for swimming pools from March through June 2026.

Serious·CPSC·Jul 23, 2026·Sviyatp

Sold nationwide. Aojieni Silicone pull string teething toys have silicone strings that are longer and smaller than safety standards allow. The strings can reach the back of a child's throat and become lodged, creating a serious choking hazard. One child experienced gagging when the strings reached their throat.

Serious·CPSC·Jul 23, 2026·Segmart