Recalls affecting North Carolina
Notices that name North Carolina in their distribution area, plus every nationwide recall — nationwide recalls reach North Carolina too.
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Class III · 11 months ago
Orthofix U.S. LLC Brand Name: Pillar" SA PTC Spacer System Product Name: Pillar" SA recall: Labeling contains claims that are not consistently present
Labeling contains claims that are not consistently present.
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Class III · 11 months ago
Orthofix U.S. LLC Brand Name: Firebird" SI Fusion System Product Name: Firebird" SI recall: Labeling contains claims that are not consistently present
Labeling contains claims that are not consistently present.
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Class II · 11 months ago
Nipro Medical Corporation Hemodialysis System, Surdial DX REF: MC+SDX01 recall: Screw may loosen or fallout of Hemodialysis system
Screw may loosen or fallout of Hemodialysis system
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Class II · 11 months ago
Medline Perfusion Syringe, REF: Dynj39223C recall: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing BD Luer Tip Caps. BD has issued a recall of…
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Class II · 11 months ago
Medline Industries, LP Dexlock Achilles Repair Implant Kits, Makt4520 recall: There have been multiple complaints of drill bit fusing to the bushing/sleeve
There have been multiple complaints of drill bit fusing to the bushing/sleeve within the drill guide during use. Retrieving a replacement drill bit…
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Class II · 11 months ago
Stryker MV3 bariatric bed recall: Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX
Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products have been sold in close…
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Class II · 11 months ago
Stryker Arise 1000EX mattress recall: Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX
Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products have been sold in close…
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Class II · 11 months ago
Bard Peripheral Vascular Inc Safe-T-Centesis 6 Fr Catheter Drainage Tray recall: Acute drainage catheters, indicated for use in removing fluid during acute
Acute drainage catheters, indicated for use in removing fluid during acute drainage/aspiration procedure, manufactured with safety indicators that…
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Class III · 11 months ago
Orthofix U.S. LLC Brand Name: Construx" Mini PTC Spacer System Product Name: Construx" recall: Labeling contains claims that are not consistently present
Labeling contains claims that are not consistently present.
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Class III · 11 months ago
Orthofix U.S. LLC Brand Name: Construx" Mini Ti Spacer System Product Name: Construx" recall: Labeling contains claims that are not consistently present
Labeling contains claims that are not consistently present.
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Class II · 11 months ago
C.R. Bard Inc BD InLay Optima Ureteral Stent Kit Size: 4.7 Fr. x 26 cm recall: Labeling discrepancy; Ureteral stent actual size may not match the actual
Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
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Class II · 11 months ago
Datascope Corp. Cardiosave Hybrid. Intra-Aortic Balloon Pump system recall: The IFU addendum revises the Preventative Maintenance schedule to align
The IFU addendum revises the Preventative Maintenance schedule to align with the update introduced in the Service Manual as of June 2023.
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Class II · 11 months ago
Cardinal Health 200, LLC ChemoPlus gowns: Product Code recall: Affected gowns have the incorrect expiration date on the product packaging
Affected gowns have the incorrect expiration date on the product packaging. Product has a shelf-life of three years which is mislabeled on the…
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Class II · 11 months ago
Beckman Coulter, Inc. Access 2 Reaction Vessels, individual, disposable recall: It has been determined that certain lots of Access 2 Reaction Vessels
It has been determined that certain lots of Access 2 Reaction Vessels may contain manufacturing deformities. The bottom (round end) of the Reaction…
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Class II · 11 months ago
C.R. Bard Inc Bard InLay Optima Size: 6 Fr. x 14 cm, Ureteral Stent Kit REF 787614 recall: Labeling discrepancy; Ureteral stent actual size may not match the actual
Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
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Class III · 11 months ago
Orthofix U.S. LLC Brand Name: Forza" Ti Spacer System Product Name: Forza" Ti Spacer recall: Labeling contains claims that are not consistently present
Labeling contains claims that are not consistently present.
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Class II · 11 months ago
C.R. Bard Inc BD InLay Optima Ureteral Stent Kit Size: 6 Fr. x 30 cm recall: Labeling discrepancy; Ureteral stent actual size may not match the actual
Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
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Class II · 11 months ago
Steris Corporation AMSCO 7053HP Washer/Disinfector Model/ recall: Wire connected to the electrical box may shift out of its intended position
Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains…
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Class II · 11 months ago
Steris Corporation AMSCO 7052HP Washer/Disinfector Model/ recall: Wire connected to the electrical box may shift out of its intended position
Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains…
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Class II · 11 months ago
Datascope Corp. Cardiosave Rescue. Intra-Aortic Balloon Pump system recall: The IFU addendum revises the Preventative Maintenance schedule to align
The IFU addendum revises the Preventative Maintenance schedule to align with the update introduced in the Service Manual as of June 2023.
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Class II · 11 months ago
Fagron Compounding Services Tropicamide 1%/Cyclopentolate 1%/Phenylephrine recall: Incorrect Product Formulation
Incorrect Product Formulation
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Class III · 11 months ago
Glenmark Pharmaceuticals Inc., USA Nebivolol Tablets, 20 mg, 90 Tablets recall: Cross Contamination with Other Products
Cross Contamination with Other Products
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Class II · 11 months ago
Cipla USA, Inc. Cinacalcet Hydrochloride Tablets, 60 mg, 30 Tablets per bottle recall: CGMP Deviations: the presence of a nitrosamine impurity
CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits.
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Class II · 11 months ago
Cipla USA, Inc. Lanthanum Carbonate chewable tablets, 1000mg* recall: Failed stability specifications: Out of specification for hardness test
Failed stability specifications: Out of specification for hardness test