Recalls affecting Montana
Notices that name Montana in their distribution area, plus every nationwide recall — nationwide recalls reach Montana too.
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Class II · 9 months ago
Cardinal Health 200, LLC Chest Drainage Units and Accessories: Product Code recall: The firm is updating the IFU to clarify the intended patient population
The firm is updating the IFU to clarify the intended patient population for the identified chest drainage units and accessories as adults, 18 years…
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Class II · 9 months ago
Philips North America Ingenia 3.0T CX. Product Code : 781271. 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
Philips North America MR 7700. Product Code : 782120 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
Philips North America Ingenia 3.0T. Product Code : 781342 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: 1) Drawer 1 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
Medline medical procedure convenience kits labeled as: Head Shave-Latex 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
Medline medical procedure convenience kits labeled as: 1) Inpatient 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. Fixone Hybrid 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
Aju Pharm Co., Ltd. Fixone Biocomposite 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
Miach Orthopaedics BEAR Implant recall: Incorrect expiration date on label that extends beyond the product's
Incorrect expiration date on label that extends beyond the product's documented/approved shelf life. With an incorrect expiration date, the UDI will…
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Class II · 9 months ago
Philips North America Evolution Upgrade 1.5T. Product Codes : 782148 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: 1) SMJ LAP Chole 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
Medline medical procedure convenience kits labeled as: 1) 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 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