South Carolina recalls

Sold nationwide. Heraeus is recalling four PALACOS bone cement product lines, which are pre-filled into mixing and application systems. The company identified a potential for the monomer liquid to leak. No injuries have been reported. The recall was distributed in the US and several other countries.

Moderate·FDA·Oct 7, 2026·Heraeus4 products

Sold nationwide. Olympus is recalling two models of its M3 Gold autoclavable telescopes, 122 units in total. The sterilization settings in the English Instructions for Use do not match those in the Japanese package insert. The recall covers units distributed only in Japan, and no injuries have been reported.

Moderate·FDA·Oct 7, 2026·Olympus2 products

Sold nationwide. Cardinal Health is recalling four Presource Pack surgical kits that contain Stryker StrykeFlow PS and AHTO tube sets. The handpieces on these tube sets may leak fluid during use, and the fluid can pool on the floor, creating a slip and fall risk. About 7,000 kits are included, and they were distributed nationwide, including in CA, IL, KY, MO, NC, NY, OH, and TX. No injuries have been reported.

Moderate·FDA·Oct 7, 2026·Cardinal Health4 products

Sold nationwide. American Contract Systems is recalling three medical convenience kits that contain BD CliniClean Pericare Wipes inside BD Urinary Catheter Trays. The wipes may be contaminated with a lubricant from the manufacturing process, which can cause localized skin irritation. About 1,804 kits of each product were affected, and the kits were distributed in Iowa, Minnesota, Wisconsin, and South Dakota. No injuries have been reported.

Moderate·FDA·Oct 7, 2026·American Contract Systems3 products

Sold nationwide. American Nitrile Operations is recalling three lines of blue nitrile patient examination gloves, covering 13 catalog numbers. The gloves may have tears, missing fingers, or debris. Defective gloves could expose health care workers and patients to infectious pathogens or chemical agents. No injuries have been reported.

Moderate·FDA·Oct 7, 2026·American Nitrile Operations3 products

Sold nationwide. United Imaging is recalling 12 models of CT and PET/CT imaging systems because of a software problem. When the Split or Local function is enabled and multiple RIS exams are merged into one study, patient images may not appear in the Patient Administration interface, which may require rescans. No injuries have been reported.

Moderate·FDA·Oct 7, 2026·United Imaging12 products

Sold nationwide. The Philips IntraSight Plus imaging system software may incorrectly link one patient's images to another patient's medical record. This could lead to wrong diagnosis or treatment if the mix-up goes unnoticed.

Moderate·FDA·Oct 7, 2026·Volcano

Sold nationwide. The EnCor EnCompass breast biopsy and tissue removal system console and driver may experience probe calibration failures or pressure sensor errors during use. When these errors occur, the system prompts the user to restart and recalibrate, which can interrupt the biopsy procedure, prolong it, or require additional tissue sampling or a repeat biopsy.

Moderate·FDA·Oct 7, 2026·Bard

Sold nationwide. Alere is recalling four groups of hCG rapid tests, which detect the pregnancy hormone hCG, because they may pick up very low hCG levels below the stated sensitivity. This can lead to a false positive result. No injuries have been reported, and the tests were sold across the U.S. and in several other countries.

Moderate·FDA·Oct 7, 2026·Alere4 products

Sold nationwide. HeartSine distributed certain models of samaritan PAD defibrillators without a required Maintenance Supplement document. This document provides instructions for an additional quarterly (every 3 months) maintenance check beyond the standard monthly check. Without these instructions, facilities may not perform the full maintenance schedule needed to keep the devices in proper working order.

Moderate·FDA·Oct 7, 2026·HeartSine

Sold nationwide. Draeger has recalled its VentStar Resus Neo neonatal breathing circuit (Part Number MP00310) due to potential cracks in the hose. These cracks could cause air leakage or allow the hose to separate during use. The recall affects all lot numbers distributed nationwide and internationally.

Serious·FDA·Oct 7, 2026·Draeger

Sold nationwide. Medline is recalling two products: hand control pendants and their wiring used with certain home care beds. The pendant or its wiring can overheat, which may cause smoking, sparking, melting, burning, or fire. About 771,127 units are affected, and the recall was expanded on 11/26/2025 to add products.

Serious·FDA·Oct 7, 2026·Medline2 products

Sold nationwide. The bolus tracking application on Philips Spectral CT 7500 scanners (Software V5.2.x) can malfunction and continue taking imaging shots even after reaching the contrast threshold. This can cause patients to receive unintended additional radiation during CT scans.

Moderate·FDA·Oct 7, 2026·Philips

Sold nationwide. Mastisol Skin Adhesive, a sterile surgical glue used in regional anesthesia procedures, is being recalled due to manufacturing issues with the product contained in surgical convenience trays. The recall affects a specific lot used in continuous epidural trays distributed nationwide.

Moderate·FDA·Oct 7, 2026·Custom Interventional Pain Management

Sold nationwide. ASP Global is recalling 64 Expressaire disposable tourniquet cuffs made between September 2016 and March 2023. The labels list a 10-year shelf life, but the validated shelf life is 5 years, so the printed expiration dates are wrong. No injuries have been reported.

Moderate·FDA·Oct 7, 2026·ASP Global64 products

Sold nationwide. Todd's Seeds is recalling six sprouting seed products because they may contain E. coli and/or Salmonella. The seeds were supplied by another company that recalled its alfalfa seed, and the affected products contain that seed. The products were sold nationwide, including through Amazon and directly to consumers, and no illnesses have been reported.

Serious·FDA·Oct 7, 2026·Todd's Seeds6 products

Sold nationwide. Apotex Corp. is recalling Paroxetine Extended-Release Tablets 37.5mg (Lot# TY9495, Exp Date 05/2027) because they failed to meet dissolution specifications. This means the tablets may not break down properly in the body, affecting how much medicine is absorbed.

Moderate·FDA·Oct 7, 2026·Apotex

Sold nationwide. Par Health USA and Endo USA are recalling certain lots of Buprenorphine Hydrochloride 0.3 mg/mL injection due to crystallization in the vials. Crystallization can affect the drug's effectiveness and safety. The recall affects six specific lots distributed nationwide.

Moderate·FDA·Oct 7, 2026·Paragon 28

Sold nationwide. A shipment of Zoladex (goserelin) 3.6 mg implants was left in an unheated FedEx trailer in outdoor conditions for approximately 25.5 hours. This temperature exposure may have affected the medication's stability and effectiveness. The recall affects 296 cartons with lot number YN0099 (expiration 01/31/2028).

Moderate·FDA·Oct 7, 2026·TerSera Therapeutics

Sold nationwide. Amneal Pharmaceuticals is recalling specific lots of Estradiol Gel 0.1% because some packets in affected cartons were found to be empty or only partially filled. This means patients may not receive the correct dose of medication. The recall affects 2,592 cartons distributed nationwide.

Moderate·FDA·Oct 7, 2026·Amneal Pharmaceuticals

Sold nationwide. Glenmark Pharmaceuticals received complaints that some cans of Clindamycin Phosphate Foam 1% arrived damaged and were leaking. The affected product was distributed nationwide. No injuries have been reported.

Moderate·FDA·Oct 7, 2026·Glenmark

Sold nationwide. Ajanta Pharma USA Inc. is recalling one lot of Ranolazine Extended-Release Tablets, 1000 mg, because the tablets failed to meet dissolution specifications. This means the medication may not release properly in the body, potentially affecting its effectiveness. The recall affects lot DJ25134 with an expiration date of 11/30/2028, distributed nationwide.

Moderate·FDA·Oct 7, 2026·Ajanta Pharma

Sold nationwide. Aurobindo Pharma USA Inc has recalled Amazon-brand Extra Strength Acetaminophen 500mg caplets due to consumer reports of discolored tablets in affected bottles. The recall affects 1000-count bottles with lot number ACD124048A and expiration date 11/30/2027 distributed nationwide.

FDA·Oct 7, 2026·Aurobindo Pharma

Sold nationwide. FDA testing found that one lot of Babies' Magic Tea Baby Sleep Gripe Water contains ethanol, methanol, and isopropanol that are not listed on the label. These alcohols can impair the central nervous system, especially in infants, and may cause drowsiness, nausea, vomiting, or more serious effects depending on how much is used.

Serious·FDA·Oct 6, 2026·Pacific Health Sciences

Sold nationwide. Leader Formulas recalled RAPTURE Preworkout powder after FDA testing found it contains DMAA, a banned stimulant ingredient. DMAA can raise blood pressure and cause heart problems, including heart attack, shortness of breath, and chest tightness.

Serious·FDA·Oct 6, 2026·Leader Formulas

Sold nationwide. A software issue in the newest StatStrip Glucose Hospital Meter (Gen 2.0 model) can cause a glucose test result to be incorrectly linked to the wrong patient's medical record. When a patient ID barcode is scanned, previous patient information may stay on the meter screen; if a healthcare worker accidentally accepts it, the test result goes to the wrong patient, potentially leading to incorrect treatment decisions. One case of inappropriate insulin administration has been reported.

Moderate·FDA·Oct 5, 2026·StatStrip

Sold nationwide. Agrish-branded adult portable bed rails (models AG-12011, AG-12014, and AG-12016) can trap users between the rail and mattress or within the rail itself, creating a serious risk of asphyxiation and death. The rails also fail safety standards for structural stability and retention straps, and have incorrectly sized push pins that can cause lacerations. About 35,000 units were sold online through Amazon from April 2025 through May 2026.

Serious·CPSC·Oct 1, 2026·Lebo

Sold nationwide. The immersion heaters in these portable camping showers can ignite when partially or completely out of water, creating a fire hazard. About 400 units were sold online through Amazon and Walmart between February and August 2026. No injuries have been reported.

Serious·CPSC·Oct 1, 2026·Golden Resale

Sold nationwide. Dollar Tree's electric balloon pump (model 406198) can overheat during use, creating a burn risk. The firm has received three reports of overheating, including one involving flames and one explosion, though no injuries have been reported so far.

Moderate·CPSC·Oct 1, 2026·Dollar Tree

Sold nationwide. Kobayashi rechargeable hand warmers contain lithium-ion batteries and electrical components that can overheat and ignite. This poses a risk of fire and serious burns to users.

Serious·CPSC·Oct 1, 2026·Kobayashi