West Virginia recalls

I.T.S. GmbH olecranon plates and olecranon hook plates used in orthopedic surgery may heat up more than expected during MRI scans under certain conditions. Updated safety testing found higher temperature increases than the original instructions stated.

I.T.S. GmbH has recalled certain Pilonplate devices used in orthopedic surgery because new MRI safety testing found they heat up more than expected during MRI scans under certain conditions. The devices affected include Anterolateral Tibia Plates, Pilon Plates 4mm, and Pilon Plates Small with specific article and lot numbers.

I.T.S. GmbH's FR.O.H. Calcaneus Repair System (anterolateral calcaneus plate, Article Number 21064-60) may heat more than expected during MRI scans under certain conditions. New testing found higher radiofrequency-induced temperature increases than the original instructions stated. Only 4 units were distributed nationwide.

I.T.S. GmbH issued a recall for certain Humeral Head Plate with Angular Stability implants used in shoulder surgery. Testing found the device may heat up more than expected during MRI scans under certain conditions. The product labeling did not reflect these updated safety findings.

I.T.S. GmbH clavicle plates used in shoulder surgery may heat up more than expected during MRI scans under certain conditions. New testing found higher temperature increases than the original instructions stated. This affects specific article numbers and lot numbers distributed across the US.

I.T.S. GmbH's Radius Plate PROlock II (a surgical implant for wrist fractures) has been recalled because new MRI safety testing found the device heats up more than the instructions said it would under certain MRI scanner conditions. The original safety information in the product labeling did not reflect these higher temperature increases.

GE Medical Systems' Imactis CT-Navigation System (Models E85101LA and E85101LP) has a potential issue where the needle's simulated path shown to the doctor may not match where the needle actually goes during CT-guided procedures. This discrepancy could affect the accuracy of needle placement during medical procedures. No injuries have been reported.

The Handy Solutions Neck & Shoulders Heating Pad (model 25607) can overheat and cause burns if folded while in use or placed under your body. When folded, the device's safety temperature sensor cannot detect the excessive heat, so it does not shut off. The pad may emit a burning smell before melting or catching fire.

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.

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.

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.

MPINOI brand adult portable bed rails can trap users between the rail and mattress, creating a serious risk of injury or death by asphyxiation. The rails also lack required warning labels. About 200 units were sold on Amazon between December 2025 and February 2026.

The electrical components in DIY Cold Plunge Sauna Heater Kits can overheat and create a fire hazard. The company has received 12 reports of units overheating, though no fires or injuries have occurred yet. The kits were sold online from March 2025 through February 2026.