Recalls in Montana (page 29)

3849 recalls.

• MEDLINE ANTERIOR HIP PACK DYNJ64672B recall (Medline Industries, LP)
  Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of...
• Medline kits containing Olympus biopsy valves: 1. BRONCH PROCEDURE KIT recall (Medline Industries, LP)
  Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of...
• Medline kits containing Olympus biopsy valves: 1. BRONCHOSCOPY recall (Medline Industries, LP)
  Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of...
• Medline kits containing Olympus biopsy valves: 1. BAL KIT recall (Medline Industries, LP)
  Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of...
• THORACIC ROBOTS recall (Medline Industries, LP)
  Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of...
• Medline convenience kits containing Olympus biopsy valves: 1. BRONCH PACK recall (Medline Industries, LP)
  Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of...
• Airway Exam Kit recall (Medline Industries, LP)
  Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of...
• Magnesium Sulfate in Water for Injection recall (Amneal Pharmaceuticals, LLC)
  DrugClass IReported April 8, 2026 · Product mix up: a foil pouch labeled "Magnesium Sulfate in Water for Injection, 4 g/100 mL" actually contained an IV bag of Tranexamic Acid instead.
• Prazosin Hydrochloride Capsules recall (Appco Pharma LLC)
  DrugClass IIReported April 8, 2026 · cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits.
• Prazosin Hydrochloride Capsules recall (Appco Pharma LLC)
  DrugClass IIReported April 8, 2026 · cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits.
• Prazosin Hydrochloride Capsules recall (Appco Pharma LLC)
  DrugClass IIReported April 8, 2026 · cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits.
• Artificial Tears Sterile Lubricant Eye Drops recall (K.C. Pharmaceuticals, Inc)
  DrugClass IIReported April 8, 2026 · Lack of Assurance of Sterility
• STERILE EYE DROPS SOOTHING TEARS recall (K.C. Pharmaceuticals, Inc)
  DrugClass IIReported April 8, 2026 · Lack of Assurance of Sterility
• Sterile EYE DROPS REDNESS LUBRICANT recall (K.C. Pharmaceuticals, Inc)
  DrugClass IIReported April 8, 2026 · Lack of Assurance of Sterility
• Sterile Eye Drops ORIGINAL FORMULA recall (K.C. Pharmaceuticals, Inc)
  DrugClass IIReported April 8, 2026 · Lack of Assurance of Sterility
• Ultra Lubricating Eye Drops recall (K.C. Pharmaceuticals, Inc)
  DrugClass IIReported April 8, 2026 · Lack of Assurance of Sterility
• Dry Eye Relief Eye Drops recall (K.C. Pharmaceuticals, Inc)
  DrugClass IIReported April 8, 2026 · Lack of Assurance of Sterility
• EYE DROPS Advanced Relief recall (K.C. Pharmaceuticals, Inc)
  DrugClass IIReported April 8, 2026 · Lack of Assurance of Sterility
• Sterile EYE DROPS AC recall (K.C. Pharmaceuticals, Inc)
  DrugClass IIReported April 8, 2026 · Lack of Assurance of Sterility
• traMADol Hydrochloride Tablets recall (Amneal Pharmaceuticals, LLC)
  DrugClass IIReported April 8, 2026 · Failed Impurities/Degradation Specifications: N-nitroso-desmethyl-tramadol impurity (NDSRI) was found out of the specification at 24-month stability interval...
• Cardinal Health Monoject Tuberculin Syringe recall (Cardinal Health 200, LLC)
  Medical deviceClass IIReported April 8, 2026 · The outer packaging and blister pack labeling identify the product as 1mL Luer Lock Tuberculin Syringe (Product Code 1180100777), however the syringes...
• SIGNA Premier systems recall (GE Healthcare LLC)
  Medical deviceClass IIReported April 8, 2026 · Whole-Body MR scanners used to produce images of the inside of the human body to aid diagnosis of disease may have been manufactured/serviced with ferrous...
• OXOID MICROBACT IDENTIFICATION KITS recall (Oxoid Australia Pty Limited)
  Medical deviceClass IIReported April 8, 2026 · Oxoid Ltd., part of Thermo Fisher Scientific, confirmed that Microbact 12L Kit 20 Tests MB1128A lot 4494873 may identify incorrect organism due to...
• Burlington Medical recall (Burlington Medical, LLC)
  Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan.
• Burlington Medical recall (Burlington Medical, LLC)
  Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan.
• Burlington Medical recall (Burlington Medical, LLC)
  Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan.
• Burlington Medical recall (Burlington Medical, LLC)
  Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan.
• Burlington Medical recall (Burlington Medical, LLC)
  Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan.
• Burlington Medical recall (Burlington Medical, LLC)
  Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan.
• Burlington Medical recall (Burlington Medical, LLC)
  Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan.
• Burlington Medical recall (Burlington Medical, LLC)
  Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan.
• Burlington Medical recall (Burlington Medical, LLC)
  Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan.
• Burlington Medical recall (Burlington Medical, LLC)
  Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan.
• Burlington Medical recall (Burlington Medical, LLC)
  Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan.
• Burlington Medical recall (Burlington Medical, LLC)
  Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan.
• Burlington Medical recall (Burlington Medical, LLC)
  Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan.
• 2.4 VOLT recall (Synthes (USA) Products LLC)
  Medical deviceClass IIReported April 8, 2026 · A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8, resulting in the bones taps having an...
• 2.4 VOLT TAP LOCKING SCREW TAP TO 90MM. Part Number: 03.424.124-US. recall (Synthes (USA) Products LLC)
  Medical deviceClass IIReported April 8, 2026 · A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8, resulting in the bones taps having an...
• Brand Name: da Vinci S recall (Intuitive Surgical, Inc.)
  Medical deviceClass IIReported April 8, 2026 · Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments
• Brand Name: da Vinci S recall (Intuitive Surgical, Inc.)
  Medical deviceClass IIReported April 8, 2026 · Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments
• Brand Name: da Vinci S recall (Intuitive Surgical, Inc.)
  Medical deviceClass IIReported April 8, 2026 · Due to increased complaints for broken/frayed grip cables for reusable instruments.
• Brand Name: da Vinci S recall (Intuitive Surgical, Inc.)
  Medical deviceClass IIReported April 8, 2026 · Due to increased complaints for broken/frayed grip cables for reusable instruments.
• Brand Name: da Vinci S recall (Intuitive Surgical, Inc.)
  Medical deviceClass IIReported April 8, 2026 · Due to increased complaints for broken/frayed grip cables for reusable instruments.
• Brand Name: da Vinci S recall (Intuitive Surgical, Inc.)
  Medical deviceClass IIReported April 8, 2026 · Due to increased complaints for broken/frayed grip cables for reusable instruments.
• Brand Name: Olympus SOLTIVE Pro SuperPulsed Laser System Product Name: SOLTIVE Pro... recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported April 8, 2026 · Following a complaint investigation, Olympus identified a potential defect in the 24V power supply module in some SOLTIVE laser units which may cause the...
• Brand Name: Olympus SOLTIVE Premium SuperPulsed Laser System Product Name: SOLTIVE... recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported April 8, 2026 · Following a complaint investigation, Olympus identified a potential defect in the 24V power supply module in some SOLTIVE laser units which may cause the...
• Sterile Radiology Procedure Kits recall (Medline Industries, LP)
  Medical deviceClass IIReported April 8, 2026 · There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility.
• Vue Motion V12. Product Number: 1017979. recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence.
• Medline Kits containing ENFIT G-TUBE CONNECTOR 1. SKU DYKM2720 G/J TUBE CARE KIT ... recall (Medline Industries, LP)
  Medical deviceClass IIReported April 8, 2026 · Connectors were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices, which could lead to leakage....
• ENFIT G-TUBE CONNECTOR recall (Medline Industries, LP)
  Medical deviceClass IIReported April 8, 2026 · Connectors were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices, which could lead to leakage....
• Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001 recall (Stryker Communications)
  Medical deviceClass IIReported April 8, 2026 · Surgical light assembly may not adequate support the weight of the ceiling cover.
• Artoura Breast Tissue Expanders Reference Numbers:... recall (Mentor Texas, LP.)
  Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
• Artoura Breast Tissue Expanders Reference Numbers:... recall (Mentor Texas, LP.)
  Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
• Artoura Breast Tissue Expanders Reference Numbers:... recall (Mentor Texas, LP.)
  Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
• CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-113TH recall (Mentor Texas, LP.)
  Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
• CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-107MH recall (Mentor Texas, LP.)
  Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
• CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-157LH ... recall (Mentor Texas, LP.)
  Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
• CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: 354-9113 recall (Mentor Texas, LP.)
  Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
• Azurion 5 M20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Azurion 5 M12 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Azurion 7 M20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Azurion 7 M12 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Azurion 7 B20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Azurion 7 B12 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Azurion 3 M15 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Azurion 3 M12 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Allura Xper FD20/15 OR Table recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Allura Xper FD20/15 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Allura Xper FD20/20 OR Table recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Allura Xper FD20/20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Allura Xper FD20/10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• ALLURA Xper FD10 OR Table recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• ALLURA Xper FD20 Biplane OR Table recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• ALLURA Xper FD20 OR Table recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• ALLURA Xper FD20 Biplane recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• ALLURA Xper FD20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• ALLURA Xper FD10/10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• ALLURA Xper FD10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• ALLURA Xper FD10F recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Allura Xper FD10C recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
• Atellica CH Enzymatic Hemoglobin A1c recall (Siemens Healthcare Diagnostics, Inc.)
  Medical deviceClass IIReported April 8, 2026 · A potential for depressed results for Atellica CH A1c_E when processing Atellica CH RCRP on the same analyzer. Customers processing A1c_E and RCRP on separate...
• Brand Name: Paradise¿ Ultrasound Renal Denervation System Product Name: Paradise ¿... recall (ReCor Medical Inc.)
  Medical deviceClass IIReported April 8, 2026 · Due to firm distributing a nonconforming product that supposed to be scrapped and not for human use.
• Brand Name: Paradise¿ Ultrasound Renal Denervation System Product Name: Paradise ¿... recall (ReCor Medical Inc.)
  Medical deviceClass IIReported April 8, 2026 · Due to firm distributing a nonconforming product that supposed to be scrapped and not for human use.
• Philips Respironics Trilogy Evo Universal recall (Philips Respironics, Inc.)
  Medical deviceClass IReported April 8, 2026 · In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
• Philips Respironics Trilogy EV300 recall (Philips Respironics, Inc.)
  Medical deviceClass IReported April 8, 2026 · In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
• Philips Respironics Trilogy Evo O2 recall (Philips Respironics, Inc.)
  Medical deviceClass IReported April 8, 2026 · In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
• Philips Respironics Trilogy Evo recall (Philips Respironics, Inc.)
  Medical deviceClass IReported April 8, 2026 · In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
• Samson International Recalls Bellevue and Oaklynn Canopy Bed Frames Due to Impact and Injury Hazards
  Consumer productReported April 3, 2026 · The canopy beams of the bed frames can collapse primarily when the bed is moved, posing impact and injury hazards to consumers.
• Tuymec Minoxidil Hair Growth Spray Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Sold on Amazon by DrHealBeauty
  Consumer productReported April 3, 2026 · The hair serum contains minoxidil, which must be in child-resistant packaging as required by the Poison Prevention Packaging Act. The hair serum's packaging is...
• Sam's Club Recalls Member's Mark Children's Pajama Sets Due to Burn Hazard; Violates Mandatory Flammability Standards for Children's Sleepwear
  Consumer productReported April 3, 2026 · The recalled pajama sets violate the mandatory standards for flammability of children's sleepwear, posing a risk of burn injuries to children.
• HTRC and Haisito T400 Battery Chargers Recalled Due to Risk of Serious Injury and Death from Fire Hazard; Manufactured by Huizhou Haitan Technology
  Consumer productReported April 3, 2026 · The chargers can ignite or cause a connected battery to ignite, posing a fire hazard and risk of serious injury and death.
• Sangohe Reannounces and Expands Adult Portable Bed Rails Recall Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails
  Consumer productReported April 3, 2026 · The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed...
• E Mishan Recalls Granitestone Diamond Pro Blue Stainless Sauté Pans Due to Impact and Burn Hazards
  Consumer productReported April 3, 2026 · The metal cap on the screw that connects the sauté pan to the handle can become detached and forcefully eject when heated, posing impact and burn hazards to...
• TecFlox Hair and Beard Growth Serum Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging
  Consumer productReported April 3, 2026 · The hair and beard growth serum contains minoxidil, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The bottles...
• ELENKER Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by Fuzhou Shiahaha Cultural Industry Development
  Consumer productReported April 3, 2026 · The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped...
• OCUN NA Recalls Condor HMS Triple Carabiners Due to Risk of Serious Injury or Death from Fall Hazard
  Consumer productReported April 3, 2026 · The carabiner's gate can malfunction where the gate does not close automatically and has to be closed manually by hand, posing a risk of serious injury or...
• Coluans Christmas Light-Up Rings Recalled Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violates Mandatory Standard for Toys; Sold on Amazon by BUDI Official
  Consumer productReported April 3, 2026 · The recalled light-up rings violate the mandatory safety standard for toys because the battery compartment within the LED light ring contains button cell...
• Gavoyeat Halloween Light-Up Rings Recalled Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violates Mandatory Standard for Toys; Sold on Amazon by CSZWEICD
  Consumer productReported April 3, 2026 · The recalled light-up rings violate the mandatory safety standard for toys because the battery compartment within the LED light ring contains button cell...
• Children's Toys Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violates the Small Ball Ban; Sold on Amazon by Beestech
  Consumer productReported April 3, 2026 · The recalled spiral tower toy sets violate the mandatory standard for toys because they contain small balls and are intended for children under three years of...
• SAVANNAH BEE COMPANY HONEY BBQ SAUCE MUSTARD recall (Savannah Bee Company Inc.)
  FoodClass IIReported April 1, 2026 · Undeclared Allergens: Soy & Wheat. The firm was notified by a customer that the product is labeled as Savannah Bee Company Honey BBQ Sauce "Mustard", but the...

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