Colorado recalls

Sold nationwide. Innovasis, Inc. is recalling certain Vector anti-torque instruments (part LS-749) used with the Vector Pedicle Screw System for spinal fusion. The instrument may be undersized, which could prevent its mating tip from engaging the pedicle screw tulip and rod during tightening. This may lead to surgical delay or the use of alternative methods to complete the final tightening step.

Moderate·FDA·Aug 12, 2026·Innovasis

Sold nationwide. Medical Action Industries is recalling Dialysis Change Tray Clear Sequence kits (model 78791) that contain a needle-free access device with an improper seal. The seal may dome or tear. No injuries have been reported.

Moderate·FDA·Aug 12, 2026·Medical Action Industries

Sold nationwide. OXOS Medical is recalling 77 MC2 and MC2.1 portable X-ray systems, software version 5.7.0, because a defective circuit board can overheat. The units were distributed in Florida, Georgia, Indiana, South Carolina, Texas, and Virginia. No injuries have been reported.

Moderate·FDA·Aug 12, 2026·Oxos Medical

Sold nationwide. munevo GmbH is recalling munevo DRIVE and munevo DRIVE r-net powered wheelchair control systems because a software issue may cause the driving mechanism to fall out of calibration. This may cause unexpected steering drift or imprecise control, and the wheelchair may veer from its intended path, possibly causing a low-speed collision, tipping, or injuries to the user or bystanders. No injuries have been reported.

Moderate·FDA·Aug 12, 2026·Munevo

Sold nationwide. Theranica Bioelectronics is recalling Nerivio Infinity devices because the battery may have a thermal runaway event during charging, which could cause smoke and odor. No injuries have been reported. The notice does not describe a fix.

Moderate·FDA·Aug 12, 2026·Theranica

Sold nationwide. Copan's WASPLab, an automated device that incubates and digitally images agar culture plates with human microbiological specimens, has a WebApp software issue. The software may prevent users from overwriting results. No injuries have been reported.

Moderate·FDA·Aug 12, 2026·Copan

Sold nationwide. Quantum Rehab is recalling 10 powered wheelchair models and controller products, including Quantum 4Front 2, Quantum Outback, Q6 Edge 3 Stretto and Quantum Rival. If the "Remind Me Later" option is selected for user reminders, reminder pop-ups may appear during use. While driving, this may cause an unexpected park brake stop that could result in a fall or injury; while not driving, the control system may crash and stay in pre-operational mode.

Moderate·FDA·Aug 12, 2026·Pride Mobility10 products

Sold nationwide. Boston Scientific is recalling three Radial Jaw 4 biopsy forceps products (Standard Capacity, Large Capacity and Jumbo) for a potential breach in the sterile barrier of the device packaging. The notice reports no injuries, and the products were distributed across the US and internationally, with international distribution still pending.

Moderate·FDA·Aug 12, 2026·Boston Scientific3 products

Sold nationwide. Integrated Medcraft is recalling two first aid kits, the FORWARD Oral Airway Kit (REF 1011-40002) and the Kingfisher Compact Individual First Aid Kit (REF 76656), that contain one-piece Guedel airway components. The devices could potentially contain an occluded or partially occluded airway tip. No injuries have been reported.

Moderate·FDA·Aug 12, 2026·Integrated Medcraft2 products

Sold nationwide. The charging cradle for the Theragun G4 PRO massage device may overheat while charging the device's removable battery pack, which presents a risk of fire. The firm has received reports that the product caught fire, as well as reports of visible smoke, melting, charger burn, burning odor, and overheating. No injuries have been reported.

Serious·FDA·Aug 12, 2026·Therabody

Sold nationwide. AVID Medical is recalling three Halyard convenience kits that contain Medline Namic Angiographic Star Off Handle Manifolds, which the manufacturer recalled because of particulates in the fluid path. The particulates could enter the bloodstream and become lodged in blood vessels. The notice lists about 5,168 affected kits for each of the three products, with distribution in the US, including NC and TX.

Serious·FDA·Aug 12, 2026·AVID Medical3 products

Peter Rabbit Organics Banana & Strawberry fruit puree pouches may contain thin, soft plastic strands from packaging defects. The affected product is a 4-ounce pouch intended for infants and young children aged 6 months and older. About 4,385 pouches from six production dates between January and May 2027 are affected.

Moderate·FDA·Aug 12, 2026·Peter Rabbit Organics

Sold nationwide. JINA F&C's Ultimate Mother's Day Wangshin Doenjang (a Korean soybean paste) was sold without listing anchovy (fish) on the allergen label, even though the product contains it. This poses a risk to people with fish allergies. The product was distributed online with best-by dates ranging from March 2027 to October 2027.

Moderate·FDA·Aug 12, 2026·JINA F&C

Sold nationwide. Ashfiat Alharamain Energy Support 250ml/8fl. oz. drinks contain undeclared tadalafil, a prescription medication used to treat erectile dysfunction. Tadalafil can cause serious health problems, especially when combined with certain other medications or in people with heart conditions. The affected product was sold nationwide through Amazon.com.

Serious·FDA·Aug 12, 2026·Ashfiat Alharamain

Sold nationwide. Big Way Hot Pot's Hot Pot Miso Paste (1kg packages) contains milk that is not declared on the label. The product was distributed to two affiliated restaurants. This poses a risk to people with milk allergies or lactose intolerance.

Moderate·FDA·Aug 12, 2026·Big Way Hot Pot

Sold nationwide. Zydus Pharmaceuticals is recalling one lot of Mirabegron Extended-Release 25 mg tablets due to higher-than-acceptable levels of N-Nitroso Mirabegron impurity. This impurity can potentially increase long-term health risks with continued use. No injuries have been reported.

Moderate·FDA·Aug 12, 2026·Zydus

Sold nationwide. Cyclophosphamide for Injection, USP (1 gram/vial) manufactured by Sunny Pharmtech Inc. for Long Grove Pharmaceuticals may contain stainless steel particulate matter. The contamination was identified in two specific lots before distribution was completed.

Serious·FDA·Aug 12, 2026·Sunny Pharmtech2 products

Sold nationwide. Aurobindo Pharma USA is recalling Dicyclomine Hydrochloride Capsules 10mg (Batch DMC125018A, expiration 07/2027) because some bottles contain empty capsules instead of the medication. The issue affects approximately 6,408 bottles distributed nationwide.

Moderate·FDA·Aug 12, 2026·Aurobindo Pharma

Sold nationwide. Schwarzkopf Professional Osis Grip extra strong mousse in 6.76 fl. oz aluminum cans may leak under pressure due to a packaging defect, creating a risk of explosion. The affected product was sold to salons and retailers across the U.S. Henkel learned of the issue through one customer complaint and two salon reports, with one instance of hand bruising reported.

Serious·FDA·Aug 11, 2026·Schwarzkopf Professional

Sold nationwide. Fresenius Kabi recalled one lot of Tyenne (tocilizumab-aazg) Injection 400 mg/20 mL vials after discovering the product contains glass particles. The affected lot was distributed nationwide to hospitals, clinics, and distributors.

Serious·FDA·Aug 10, 2026·Fresenius Kabi

Sold nationwide. The USDA found that multiple meat and poultry products contain jalapeños contaminated with Salmonella bacteria. The contaminated jalapeños came from an FDA-regulated supplier. No illnesses have been reported yet, but the products are being recalled out of caution.

Serious·USDA·Aug 8, 2026

Sold nationwide. City Foods, Inc. is recalling ready-to-eat pastrami and corned beef products because they may be contaminated with Listeria, a bacterium that can cause serious illness. The contamination was discovered during routine testing.

Serious·USDA·Aug 8, 2026·Midamar

Sold nationwide. Lexunder Inc., doing business as Food To Live, is recalling multiple green powder products (wheatgrass, spirulina, algae mix, and SuperGrass powders) because they may be contaminated with Salmonella. The company learned of the potential contamination after the FDA tested a retail sample. No illnesses have been reported so far.

Serious·FDA·Aug 7, 2026·Lexunder

Sold nationwide. Certain Apeks second stage scuba regulators (models XL4, XL4+, and XL4 Ocea) can restrict air flow to divers at depths beyond 147 feet, creating a serious breathing hazard underwater. The affected regulators were sold between April 2025 and June 2026 and can be identified by serial numbers laser-etched on the side of the equipment.

Serious·CPSC·Aug 6, 2026·Head

Sold nationwide. Fitueyes' Laziza wooden dressers can tip over if not anchored to the wall, creating a serious hazard for children. The dressers don't meet federal safety standards for furniture stability. About 150 units were sold online through Wayfair from March 2024 to April 2026.

Serious·CPSC·Aug 6, 2026·Fitueyes

Sold nationwide. The spliced ends on certain Courant Spliced Kalimba climbing ropes can fail unexpectedly during use. These ropes are designed for tree climbing and arborist work. The manufacturer has received three reports of splice failures, though no injuries have been reported yet.

Serious·CPSC·Aug 6, 2026·Courant

Sold nationwide. KC Imports Mini Laser Pointer Keychains contain button cell batteries that children can access and swallow. Ingesting these batteries can cause serious internal injuries, chemical burns, and death. The product also lacks required safety warnings.

Serious·CPSC·Aug 6, 2026·KC Imports and Exports

Sold nationwide. Syera LED finger light toys sold on Temu contain button cell batteries that children can easily access and swallow. Ingesting these batteries can cause serious internal chemical burns and other life-threatening injuries.

Serious·CPSC·Aug 6, 2026·Syera

Sold nationwide. The silicone pull strings on this teething toy are longer and thicker than safety standards allow. The strings can reach the back of a child's throat and become lodged, causing choking or difficulty breathing. One child has already been injured this way.

Serious·CPSC·Aug 6, 2026·Okabesini

Sold nationwide. EEMB lithium coin battery chargers contain easily accessible batteries that are not in child-resistant packaging and lack required safety warnings. If swallowed, these small batteries can cause serious internal burns and death.

Serious·CPSC·Aug 6, 2026·A2batt