Utah recalls

Merit Medical Systems is recalling certain BioFlo DuraMax Catheters because the sheath introducer may not split as designed. This defect could lead to complications during medical procedures, including bleeding, blood clots, or difficulty removing the catheter.

Merit Medical Systems is recalling certain DuraMax chronic hemodialysis catheters due to a design defect in the 16F dual-valved splittable sheath introducer. The sheath may not split properly during insertion, which could cause bleeding, blood clots, catheter malfunction, or loss of future vascular access.

Merit Medical Systems is recalling specific lots of its 16F dual-valved splittable sheath introducer because of a design defect that may prevent it from splitting properly during use. This could lead to serious complications including bleeding, blood clots, or damage to blood vessels.

Merit Medical Systems is recalling certain ProGuide Chronic Dialysis Catheters with a 16F dual-valved splittable sheath introducer due to a design defect. The sheath may not split as intended during insertion, which could cause serious complications including bleeding, blood clots, or damage to blood vessels.

Merit Medical Systems is recalling certain CentrosFLO hemodialysis catheters because the introducer sheath may not split properly during placement. This design defect could lead to bleeding, blockages, or difficulty placing the catheter correctly.

Erbe USA Inc is recalling specific lots of Flexible Cryoprobe devices used in surgery because the probes may rupture or burst when activated. This defect could affect patient safety during the procedure. No injuries have been reported to date.

Erbe USA Inc. is recalling certain Flexible Cryoprobe surgical devices (model OD 1.7mm, L1.15mm, REF: 20402-410) because the probes may rupture or burst when activated during surgery. This defect could cause injury to patients or surgical staff. No injuries have been reported so far.

Erbe USA has recalled certain flexible cryoprobes used in surgery because they may rupture or burst when activated. The defect could cause unexpected device failure during a procedure. No injuries have been reported, but the risk requires immediate action.

SiluetaYa Mexican Tejocote Roots Supplement Pieces contain yellow oleander, a toxic plant that can cause serious illness. The affected product was sold online in Arizona, California, New Mexico, New York, Texas, and Utah. This is a Class I recall, the FDA's most serious category.

Nuts.com Espresso Malted Milk Balls contain wheat and soy allergens that are not listed on the package label. The ingredient soy lecithin contains soy, and wheat is also present in the product. People with wheat or soy allergies could have a serious reaction if they eat this product.

Tops GOLD Green Chilli Pickle (31.74 oz cans) may contain higher-than-allowed levels of erucic acid from the mustard oil ingredient. Erucic acid in high amounts can pose health risks. The affected product was distributed in California, Nevada, Oregon, Utah, and Washington.

Tops GOLD Stuffed Red Chilli Pickle (31.74 oz cans) may contain elevated levels of erucic acid from the mustard oil ingredient. Erucic acid in high amounts can pose health risks with prolonged consumption. The affected product was distributed in California, Nevada, Oregon, Utah, and Washington.

Tops GOLD Khatta Meetha Pickle (33.51 oz cans) may contain high levels of erucic acid, a harmful substance sometimes found in mustard oil. The affected product was distributed in California, Nevada, Oregon, Utah, and Washington. No injuries have been reported.

Tops GOLD Lime Pickle (31.74 oz cans, made in India) may contain elevated levels of erucic acid from the mustard oil ingredient. Erucic acid in high amounts can pose health risks if consumed regularly. The recall affects 40 cases distributed in California, Nevada, Oregon, Utah, and Washington.

Tops GOLD Mango Pickle made with mustard oil may contain elevated levels of erucic acid, a compound that can pose health risks if consumed regularly in high amounts. The recalled products were distributed in California, Nevada, Oregon, Utah, and Washington. No illnesses have been reported.

Tops GOLD Mixed Pickle may contain erucic acid from the mustard oil ingredient. Erucic acid can be harmful if consumed in high amounts over time. This recall affects two sizes sold in the Western U.S.

American Laboratories is recalling Pepsin 1:3000 Powder (Item #FTI-G0193-00, Lot Code 00160041) because it may be contaminated with Salmonella. The affected powder was distributed to wholesale accounts in multiple states and Australia. No illnesses have been reported so far.

American Laboratories is recalling Pepsin 1:10,000 Powder (Item #FTI-G0193-00, Lot Code 00560021) due to potential Salmonella contamination. The affected product was distributed to wholesale accounts in multiple states and Australia. No illnesses have been reported.

American Laboratories is recalling Pepsin Full Strength Powder (Item #5000545, Lot Code 29460025) due to potential Salmonella contamination. The affected product was distributed to wholesale accounts in multiple states and Australia. No illnesses have been reported.

Bulk packaged dietary ingredient manufacturer product label does not declare Milk as an allergen ingredient.

Western Mixers Produce & Nuts, Inc. is recalling Treasured Harvest brand Chilli Spanish Peanuts (25lb bag, lot #260230, expiration 1/23/2027) because glass fragments were found inside a sealed container. One case has been distributed to retail locations across the country.

Western Mixers Produce & Nuts found glass inside sealed containers of First Street Chilli Spanish Peanuts (11oz). The affected products have lot numbers 260422, 260442, or 260543, with expiration dates between February 11–23, 2027. No injuries have been reported.

American Health Packaging is recalling specific batches of Meclizine Hydrochloride 12.5 mg tablets because they failed to meet required tablet specifications. The affected product is Lot #1024852 with an expiration date of 9/30/2026. No injuries have been reported.

Teva Pharmaceuticals is recalling specific lots of Octreotide Acetate 30 mg injectable suspension due to quality control problems found at the manufacturer. The FDA identified deficiencies that mean the sterility of these vials cannot be guaranteed. No injuries have been reported.

Teva Pharmaceuticals is recalling specific lots of Octreotide Acetate injectable suspension (20 mg) due to quality control issues at the manufacturing facility in Greece. The FDA found deficiencies that could affect sterility—the assurance that the medication is free from harmful bacteria and other microorganisms.

Teva Pharmaceuticals is recalling specific lots of Octreotide Acetate injectable suspension due to sterility concerns identified at the manufacturing facility. The FDA found quality system deficiencies that could affect the safety of the medication.

Macleods Pharma USA is recalling Levothyroxine Sodium Tablets USP 150 mcg because they may contain less active ingredient than labeled. This means the medication may not work as intended to treat thyroid conditions. The affected lot is 16240062A with an expiration date of March 2026.

Chiesi USA is recalling specific lots of CUROSURF, a medication given to premature infants to help them breathe. The company cannot confirm that all vials are sterile, which means they may be contaminated. No infections have been reported so far.

Radnostix Gelatin Capsule Packs used with Sodium Iodide I-131 Kit have failed quality specifications. The affected capsules may not perform as intended. Three specific lots distributed nationwide are involved.

Kian Pee Wan capsules, sold online as a dietary supplement for weight gain and appetite, contain two hidden prescription drugs: dexamethasone (a corticosteroid) and cyproheptadine (an antihistamine). These drugs were not listed on the label. Taking these undeclared drugs can cause serious health problems including infections, high blood sugar, psychiatric issues, and withdrawal symptoms if stopped abruptly.