Recalls affecting Nebraska
Notices that name Nebraska in their distribution area, plus every nationwide recall — nationwide recalls reach Nebraska too.
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Class I · 9 months ago
SunMed Holdings, LLC Brand Name: Broselow Product Name: Broselow Pediatric Emergency recall: Product contains potentially harmful dosing errors for Vecuronium
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
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Class II · 9 months ago
Siemens Medical Solutions USA, Inc Interventional Fluoroscopic X-Ray System: Luminos recall: Ortho images acquired with preset automatic horizontal flip are not flipped
Ortho images acquired with preset automatic horizontal flip are not flipped and when acquiring single images, there is the possibility that an image…
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Class II · 9 months ago
Philips North America Ingenia Ambition S. Product Code : 782108. MR systems with SW recall: The potential for stiffness value errors when viewing exported MR
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication…
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Class II · 9 months ago
Aju Pharm Co., Ltd. Genesis Push-In Suture Anchor recall: Reports of device failure, including anchor breakage, anchor bending
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
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Class II · 9 months ago
Philips North America SmartPath to dStream for 3.0T. Product Code : 782145. MR systems recall: The potential for stiffness value errors when viewing exported MR
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication…
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Class II · 9 months ago
Medline medical procedure convenience kits labeled as: Nerve Block Tray recall: Medline kits were manufactured and distributed containing MASTISOL liquid
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing…
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Class II · 9 months ago
Aju Pharm Co., Ltd. AlternatiV+ Screw-In Anchor recall: Reports of device failure, including anchor breakage, anchor bending
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
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Class II · 9 months ago
Medline medical procedure convenience kits labeled as: 1) Watkins Spine recall: Medline kits were manufactured and distributed containing MASTISOL liquid
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing…
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Class II · 9 months ago
LSL Healthcare, Central Line Dressing Kit, Model/ recall: BD ChloraPrep Triple Swabsticks, a component within the kits
BD ChloraPrep Triple Swabsticks, a component within the kits, exhibit an open seal on the packaging of the applicators.
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Class II · 9 months ago
Greenstone Llc methylprednisolone tablets, USP Dosepak, 4 mg recall: Labeling: Not Elsewhere Classified. Incorrect orientation of the blister foil
Labeling: Not Elsewhere Classified. Incorrect orientation of the blister foil applied to the blister cavities, which results in incorrect dosing…
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Class III · 9 months ago
Novadoz Pharmaceuticals LLC Glycopyrrolate Oral Solution, 1 mg/5 mL, 16 oz recall: Failed Impurities/Degradation Specifications
Failed Impurities/Degradation Specifications
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Class II · 9 months ago
Baxter Healthcare Corporation Sterile Water for Irrigation, 250 mL recall: Presence of particulate matter: plastic particles from the bottle rim
Presence of particulate matter: plastic particles from the bottle rim were observed floating into the solution
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Class III · 9 months ago
Haleon US Holdings LLC parodontax Active GUM Health, Mouthwash, Mint recall: Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for missing
Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for missing or illegible lot and expiration date coding on the bottles.
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NHTSA safety recall · 9 months ago
Chrysler recall: Due to an improperly designed trailer tow module
Due to an improperly designed trailer tow module, the trailer lights may fail to illuminate and the trailer brakes may fail.
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Elevated risk · 9 months ago
Hyena, Inc. Rear wheel bolts installed on model year 2026 Trek FX+ 1 and Electra recall: The rear wheel bolts can break when torqued
The rear wheel bolts can break when torqued, causing the wheel to separate from the bicycle, posing a fall hazard.
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Highest risk · 9 months ago
Northern Tool + Equipment Hot Water Pressure Washers recall: Fire Hazard
Fire Hazard
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Highest risk · 9 months ago
Hobby Lobby Giraffe and Llama Plush Toys with Clips recall: Choking Hazard
Choking Hazard
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Highest risk · 9 months ago
Bazic Silicone Glue recall: Risk of Serious Injury or Death from Child Poisoning
Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child Resistant Packaging and FHSA Labeling Requirements
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Elevated risk · 9 months ago
Neogen Vet Hycoat® Hyaluronate Sodium Sterile Solution recall: Microbial Contamination
Microbial Contamination
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Class I · 9 months ago
Ashfiat Alharamain Honey Product for Energy Support recall: Product contains tadalafil
Product contains tadalafil
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Highest risk · 9 months ago
Why Not Natural Organic Moringa – Green Superfood recall: Potential Foodborne Illness - Salmonella
Potential Foodborne Illness - Salmonella
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NHTSA safety recall · 9 months ago
Toyota recall: Water may enter the rear door switch and cause a short circuit
Water may enter the rear door switch and cause a short circuit, allowing an unlocked rear door to open unexpectedly.
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Class II · 9 months ago
GVS TM, Inc SQ40S Blood Transfusion Filter recall: Due to products being released for distribution prior to completion
Due to products being released for distribution prior to completion of the required quality control release process the sterility assurance cannot be…
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Class II · 9 months ago
Brand Name: EDAN Product Name: Patient Monitor Model/ recall: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm…