Colorado recalls

Sold nationwide. The tempered glass window on the pizza oven of this grill can shatter during use, creating a laceration hazard. Conair has received 37 reports of the glass shattering and one report of fire; no injuries have been reported so far.

Serious·CPSC·Jul 9, 2026·Cuisinart

Sold nationwide. Zimmer Biomet is recalling two A.T.S 4000 TS tourniquet system hoses because the sealing area of the sterile pouch may be breached. If used, the hose may cause a moderate, localized infection. If found before use, surgery may be briefly extended while another device is located.

Moderate·FDA·Jul 8, 2026·Zimmer Biomet2 products

Sold nationwide. W L Gore & Associates has recalled specific batches of the GORE TAG Thoracic Branch Endoprosthesis Side Branch Component due to a risk of catheter separation during use. This is a surgical implant used to repair certain aortic conditions. The separation could potentially affect the device's ability to function as intended.

Moderate·FDA·Jul 8, 2026·Gore

Sold nationwide. Masimo is recalling two Radius VSM products: an ECG pre-connected electrode set and disposable blood pressure cuffs, covering 1,800 units in total. The ECG feature may incorrectly flag abnormally slow or fast heart rates in patients with normal rhythms, which could distract clinicians from true alarms and delay treatment. The blood pressure cuffs may have rough edges that can cause skin irritation or redness. No injuries have been reported.

Moderate·FDA·Jul 8, 2026·Masimo Corporation2 products

Sold nationwide. Laborie Medical Technologies' Solar GI System water perfusion devices may accumulate moisture inside tubing, filters, and pressure sensors during extended clinical use. This moisture buildup can affect how the system measures airflow and pressure, potentially impacting test results.

Moderate·FDA·Jul 8, 2026·Laborie Medical Technologies Corp

Sold nationwide. Bard Access Systems is recalling 14 products, including PICC, midline, and dialysis catheters and biopsy trays. The recall stems from lidocaine ampoules that were made under deficient manufacturing practices, and the supplier is recalling them. No injuries have been reported.

Moderate·FDA·Jul 8, 2026·Bard14 products

Sold nationwide. The Shiley Disposable Decannulation Plug (DDCP), a red connector used on tracheostomy tubes to block airflow, carries labeling that incorrectly indicates it does not contain DEHP (a chemical compound). The product actually contains 30–35% DEHP. Users relying on the label may not be aware of DEHP exposure during use.

Moderate·FDA·Jul 8, 2026·Covidien LLC

Sold nationwide. Certain Zeiss Intrabeam Spherical Applicator 1.5 cm units used in intraoperative radiation therapy did not meet manufacturing specifications. A total of 13 units were affected across the United States, Puerto Rico, and several other countries. No injuries have been reported.

Moderate·FDA·Jul 8, 2026·Carl Zeiss Meditec

Sold nationwide. Siemens has identified a potential issue with the Display ceiling suspension (DCS Fix XL) component on ARTIS icono ceiling systems. Over time, screws that secure the monitor to the suspension may gradually loosen, which could affect the stability of the mounted display.

Moderate·FDA·Jul 8, 2026·Siemens

Sold nationwide. RayCare 2024A SP1 oncology information system has a software issue where beam set delivery notes can lose data if modified at the same time or updated during an active treatment session. Users may not be notified when these changes occur, potentially affecting treatment records.

Moderate·FDA·Jul 8, 2026·Raysearch Laboratories2 products

Some Medela ENFit ExSet enteral extension sets contain incorrect connectors that may not attach properly to ENFit connections. This incompatibility could cause a slight delay in delivering nutrition or medication through the feeding tube.

Moderate·FDA·Jul 8, 2026·Medela Inc

Sold nationwide. In some cases, the collimator (a precision component) may not fully dock into the Cyberknife treatment system. This triggers a safety interlock that blocks motion from the operator console. However, if staff enter the treatment room and use the in-room control pendant to move the system, the collimator can release and fall from its housing, creating a potential impact hazard.

Moderate·FDA·Jul 8, 2026·Accuray Incorporated

Sold nationwide. Siemens is recalling three models of its ARTIS icono imaging systems, 234 units in total, because the detector lift may stop moving after it is adjusted to its highest or lowest height limit. No injuries have been reported.

Moderate·FDA·Jul 8, 2026·Siemens3 products

Sold nationwide. In some cases, the collimator (a precision component) may not fully dock into the Cyberknife system. If operators bypass the safety interlock by using the in-room control pendant, the collimator can release and fall from the machine housing. This affects 48 Cyberknife units worldwide running software version 11X or earlier.

Moderate·FDA·Jul 8, 2026·Accuray Incorporated

Sold nationwide. Pilling Wecksorb Neurosponges—sterile cotton sponges used during brain and spine surgery—may contain higher-than-safe levels of endotoxins (bacterial toxins). The affected sponges were manufactured between 2021 and 2024. No injuries have been reported, but elevated endotoxins could trigger an inflammatory response during surgery.

Moderate·FDA·Jul 8, 2026·TELEFLEX LLC

Sold nationwide. The Adapter for Head Positioning (Model 1739994) used with Baxter operating tables may become loose during patient positioning and move unintentionally. This affects 13 units distributed worldwide, primarily in Minnesota, Maryland, Pennsylvania, Canada, and numerous other countries.

Moderate·FDA·Jul 8, 2026·Baxter

Sold nationwide. Boston Scientific is recalling 12 sizes of its CRE and CRE Pro Wireguided balloon catheters because the pouches they are packaged in may not keep the devices sterile. The recall covers 81,543 units per product and was distributed in the US and many other countries. No injuries have been reported.

Moderate·FDA·Jul 8, 2026·Boston Scientific12 products

Sold nationwide. The IntelliCuff portable cuff pressure controller may display a "Cuff System Leakage" error and cause the motor to pump continuously instead of maintaining the pressure set by the user. This can prevent the device from working as intended.

Moderate·FDA·Jul 8, 2026·Hamilton Medical AG

Sold nationwide. Certain lots of the Medtronic Harmony Delivery Catheter System may have a manufacturing defect that increases the risk of the distal tip detaching from the delivery system during use. This could occur under specific procedural or anatomical conditions. About 1,881 units worldwide are affected.

Serious·FDA·Jul 8, 2026·Medtronic Heart Valves Division

Sold nationwide. Remel, Inc. is recalling certain 100mm and 150mm GC Agar Base lab culture plates because some strains of gonorrhea bacteria may grow poorly or not at all on them. The recall covers specific lot numbers and was distributed in the US, Canada, Singapore, and the United Kingdom. No injuries have been reported.

Moderate·FDA·Jul 8, 2026·Remel

Sold nationwide. Windstone Medical Packaging is recalling four Aligned Medical Solutions surgical convenience kits, 1,525 units in total. The kits contain Webcol Large Alcohol Prep Pads that Cardinal Health recalled after a bacterium, Paenibacillus phoenicis, was found during a routine sterilization audit. The kits were distributed nationwide, with confirmed distribution in PA, GA, CA, and WA. No injuries have been reported.

Serious·FDA·Jul 8, 2026·Windstone Medical Packaging4 products

Sold nationwide. Medacta's Short Monobloc Stem Broaches (sizes 7–16), used during shoulder replacement surgery, have a manufacturing issue that causes the surgical instruments to be positioned slightly off-center during the procedure. This misalignment may increase the risk of fractures in the upper arm bone.

Moderate·FDA·Jul 8, 2026·Medacta Usa Inc

Sold nationwide. Certain lots of DePuy Synthes ATTUNE Revision Hinge Knee Insert components were found with external sterile packaging adhered to the internal sterile packaging. This contact may have compromised the sterility of the surgical implant inside.

Moderate·FDA·Jul 8, 2026·DEPUY (IRELAND)2 products

Sold nationwide. Specific lots of Medline reprocessed St. Jude Medical Response diagnostic electrophysiology catheters may contain small particles of residual material on surfaces that contact patients. If these particles dislodge during use, they could potentially cause blood clots, inflammation, or infection.

Serious·FDA·Jul 8, 2026·Medline

Sold nationwide. Medline is recalling 8 convenience kits that contain Swan-Ganz catheters made by Becton Dickinson (BD). BD received complaints that the blue hub on these catheters can leak or break, which may lead to infection, medication loss, or blood loss. No injuries have been reported, and the kits were distributed in AZ, CA, FL, IL, MO, NJ, OH, OK, TN, TX, and WI.

Moderate·FDA·Jul 8, 2026·Medline8 products

Sold nationwide. Insulet is recalling three Omnipod pod lines (Omnipod 5, Omnipod DASH, and Omnipod Eros), about 7 million units in total. Damage to the soft cannula during manufacturing can let insulin leak around the pod instead of being delivered, so users may get too little insulin. This can cause high blood sugar, and in severe cases prolonged high blood sugar can lead to diabetic ketoacidosis, hyperglycemic hyperosmolar syndrome, or death. No injuries have been reported.

Serious·FDA·Jul 8, 2026·Insulet3 products

Sold nationwide. Four Hillrom VOLARA System patient circuit kits are included in this recall. Air and medication can leak from the nebulizer cup during therapy, which can lower a patient's oxygen level and make the treatment less effective. The problem has been linked to the nebulizer cup not being locked properly after medication is added during setup. No injuries have been reported.

Serious·FDA·Jul 8, 2026·Baxter4 products

Sold nationwide. Medline is recalling 15 convenience kits that contain Huons lidocaine ampules. Huons issued the recall after an FDA inspection of its manufacturing site found quality problems with the ampules. No injuries have been reported.

Moderate·FDA·Jul 8, 2026·Medline15 products

Sold nationwide. Certain coaxial breathing circuit sets used with Hamilton Medical ventilators (models C1, T1, and MR1) may have expiratory valve membranes that stick to the valve body. This defect is not always detectable before use and can trigger an "exhalation obstructed" alarm during ventilation, potentially leading to inadequate ventilation and oxygen desaturation in patients.

Serious·FDA·Jul 8, 2026·Hamilton Medical AG

Sold nationwide. Nara Organics Whole Milk Organic Infant Formula in two sizes may be contaminated with Clostridium botulinum, a bacterium that can cause botulism. The contamination was identified in specific lot codes with use-by dates between March 2027 and February 2028. No illnesses have been reported.

Serious·FDA·Jul 8, 2026·nara organics