Alabama recalls

The proximal clasp on Bolton Medical's RelayPro Thoracic Stent-Graft System may disconnect from the outer control tube during use. This disconnection could prevent the stent graft from being released properly from its delivery system. The FDA has issued a labeling update to inform physicians and hospitals of this potential issue.

Fly By Jing Creamy Sesame Noodles (3.8 oz packets) may contain peanuts due to cross-contamination during production, even though peanuts are not listed on the label. This poses a serious risk to people with peanut allergies. The recall affects approximately 3,419 cases with best-by dates between October 15, 2026 and March 23, 2027.

AbbVie is recalling specific lots of PRED MILD (prednisolone acetate) eye drops because they failed stability testing. The affected product may not maintain its intended strength or safety over time. Two lots are involved, with an expiration date of August 2026.

AVEVA nicotine patches (14 mg) distributed by Rugby Laboratories have elevated levels of chemical impurities that exceed safety standards for shelf life. The issue was discovered during stability testing of specific lots. No injuries have been reported.

Champion Foods is recalling certain batches of Motor City Pizza Co. 5 Cheese Bread because a milk powder ingredient supplied by California Dairies may be contaminated with Salmonella. The contamination was found in the milk powder used to make the seasoning blend, though no illnesses have been reported so far.

Better Weather Actives LLC is recalling all lots of Better Weather Fix Elixir 15 ml because the product may contain undeclared Mitragynine and Mitragynine Pseudoindoxyl, which are kratom alkaloids. These substances can cause serious effects including nausea, vomiting, rapid heart rate, hallucinations, and in severe cases, respiratory depression or loss of consciousness.

Mainstays 9-drawer fabric dressers sold at Walmart can tip over if not anchored to the wall, creating a risk of serious injury or death to children. The dressers do not meet federal safety standards for clothing storage units. About 165,000 units are affected.

These glowing fidget spinner balls come with a mini flashlight that contains two small button cell batteries. The batteries are easy for children to remove and swallow. Swallowed button batteries can cause serious internal injuries and death.

The battery compartment screw on these rackets does not stay attached when opened, allowing children to easily access button cell batteries inside the shuttlecock. Swallowed button cell or coin batteries can cause serious internal injuries, including chemical burns, and can be fatal.

Giantex outdoor lounge chairs (model NP10025NY) have a pinch point that can trap and amputate fingers when the backrest is adjusted. One person has already lost a finger this way. About 1,155 chairs were sold online between August 2023 and October 2025.

Tzumi Electronics' SLF Sauna Blankets (model 30065TAR) can overheat during use, creating fire and burn risks. The company has received six reports of overheating, including five cases of minor furniture damage. About 3,600 units were sold through Target, Macy's, Snappy, and online from February 2025 through February 2026.

Panasonic-branded VL2020 lithium coin batteries sold online were packaged in clear plastic bags without child-resistant packaging or required warning labels. If swallowed, coin batteries can cause serious internal burns and death within hours.

Daoen Inc. is recalling Zen-branded magnetic ball fidget toys because the high-powered magnets inside can be swallowed by children. When multiple magnets are ingested, they can attract each other and become stuck in the digestive system, potentially causing serious internal injuries or death.

These small disc magnets are too powerful and too small, violating federal safety rules. If swallowed, multiple magnets can attract each other inside the stomach and intestines, causing perforations, blockages, and serious internal injury or death.

The steam diffuser in these portable saunas can be positioned too close to your body, allowing hot steam to contact your skin. Giantex has received nine reports of burns, including one second-degree burn.

SkinnyDipped Dark Chocolate Coconut Almond Bites in certain lots may contain undeclared peanut or peanut butter, even though peanuts are not an intended ingredient. The issue was discovered after a consumer found peanut butter–containing products in the wrapper. People with peanut allergies could have a serious allergic reaction.

A rubber hose inside the X-ray tube cooling unit (type CU3101) on certain Philips Integris-Allura systems can degrade and leak oil over time. This reduces cooling performance and causes the system to automatically switch to low-dose mode with a "Tube cooler problem" message that cannot be cleared by restarting. The affected cooling units were manufactured between February 2016 and May 2020.

A cooling hose in certain Philips Allura X-ray systems manufactured between February 2016 and May 2020 may degrade over time and leak oil. If oil leakage reduces cooling performance below a safe threshold, the system automatically switches to low-dose fluoroscopy and cannot be fixed by restarting.

A cooling hose in certain Philips Azurion X-ray systems may degrade over time and leak oil, reducing cooling performance. When oil levels drop too far, the system automatically switches to low-dose mode and cannot be fixed by restarting.

Certain Philips Azurion fluoroscopy systems may experience mechanical wear in the Float Tabletop control, which could impair the longitudinal and transverse (side-to-side and front-to-back) movement of the examination table. This wear could affect the system's ability to position patients correctly during imaging procedures.

Certain lots of Medtronic DLP Retrograde Cannula (Model 94965), a cardiopulmonary bypass catheter, may have a breach in the sterile barrier that protects the device before use. This affects 260 units distributed worldwide, including in the United States.

Certain lots of the Medtronic DLP Retrograde Cannula (Model 94915), a catheter used during heart bypass surgery, may have a breach in their sterile packaging. This could allow contamination before the device is used. No injuries have been reported.

Certain lots of Medtronic DLP Retrograde Cannula (Model 94913L), a catheter used in heart surgery, may have a compromised sterile barrier. This could allow contamination during the surgical procedure. The issue affects 481 units distributed worldwide.

Certain lots of Medtronic DLP Retrograde Cannula (Model 94913), a catheter used in heart-lung bypass surgery, may have a compromised sterile barrier. This could allow contamination before use. The affected product was distributed worldwide, including the United States.

Certain lots of Medtronic DLP Retrograde Cannula (Model 94725), a catheter used in heart surgery, may have a breach in their sterile packaging. This could potentially expose the device to contamination before use. The affected lots have been identified by lot number and GTIN code.

Certain lots of Medtronic DLP Retrograde Cannula (Model 94665) used in heart-lung bypass surgery may have a compromised sterile barrier. This could allow contamination of the device before use. The affected lots have been identified and distributed worldwide.

Certain lots of Medtronic DLP Retrograde Cannula (Model 94215T), a catheter used during heart surgery, may have a compromised sterile barrier. This affects 600 units distributed worldwide. No injuries have been reported.

Certain lots of Medtronic GUNDRY Retrograde Cannula (Model 94115T), a catheter used during heart-lung bypass surgery, may have a breach in their sterile packaging. This could allow contamination of the device before use. The affected lots have been identified and are listed in the recall notice.

Certain lots of Medtronic GUNDRY Retrograde Cannula (Model 94113T), a cardiopulmonary bypass catheter, may have a breach in the sterile barrier. This could allow contamination of the sterile product before use during heart surgery.

The straight inserter tool on certain OneLIF Interbody Cage implants may fail to attach properly to the cage. This could prevent secure engagement during spinal fusion surgery, potentially causing procedural delays or requiring surgeons to choose a different implant.