Recalls affecting Virginia
Notices that name Virginia in their distribution area, plus every nationwide recall — nationwide recalls reach Virginia too.
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Class II · 10 months ago
Zimmer, Inc. Brand Name: Affixus Antegrade Femoral Nailing System Product Name recall: Affected implants may have undersized distal diameter along length
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk…
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Class II · 10 months ago
Zimmer, Inc. Brand Name: Affixus Antegrade Femoral Nailing System Product Name recall: Affected implants may have undersized distal diameter along length
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk…
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Class II · 10 months ago
Zimmer, Inc. Brand Name: Affixus Antegrade Femoral Nailing System Product Name recall: Affected implants may have undersized distal diameter along length
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk…
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Class II · 10 months ago
Zimmer, Inc. Brand Name: Affixus Antegrade Femoral Nailing System Product Name recall: Affected implants may have undersized distal diameter along length
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk…
-
Class II · 10 months ago
Zimmer, Inc. Brand Name: Affixus Antegrade Femoral Nailing System Product Name recall: Affected implants may have undersized distal diameter along length
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk…
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Class II · 10 months ago
Intuitive Surgical, Inc. da Vinci 5, Surgeon Console Column Motor Connector recall: Surgical system Error 23062 due to connector1) Partially damaged "Potential
Surgical system Error 23062 due to connector1) Partially damaged "Potential problem with ergonomics: Disable - Retry " or 2) Failed "Disable…
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Class II · 10 months ago
Brand Name: Diasol Product Name: 100220-10-DEX100 recall: Safety and efficacy of dialysis acid concentrate cannot be assured
Safety and efficacy of dialysis acid concentrate cannot be assured
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Class II · 10 months ago
Brand Name: Diasol Product Name: 100225-10-DEX100 recall: Safety and efficacy of dialysis acid concentrate cannot be assured
Safety and efficacy of dialysis acid concentrate cannot be assured
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Class II · 10 months ago
Brand Name: Diasol Product Name: 100425-10-DEX100 recall: Safety and efficacy of dialysis acid concentrate cannot be assured
Safety and efficacy of dialysis acid concentrate cannot be assured
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Class II · 10 months ago
Microbiologics Inc Kwik-Stik 2-Pack, Campylobacter jejuni subsp. jejuni derived recall: Affected units may fail to recover the target microorganism Campylobacter
Affected units may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni derived from ATCC 29428.
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Class I · 10 months ago
Draeger Vapor 2000. Unheated, calibrated anesthetic vaporizer recall: A certain component of affected devices was not delivered within
A certain component of affected devices was not delivered within specification and contained impurities.
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Class II · 10 months ago
Zimmer, Inc. Brand Name: Affixus Antegrade Femoral Nailing System Product Name recall: Affected implants may have undersized distal diameter along length
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk…
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Class II · 10 months ago
Howmedica Osteonics Corp. The Stryker CranialMask Tracker is a single-use device recall: When the device is activated during surgery
When the device is activated during surgery, the device software issues an error message "Instrument Face Mask (6001385000000) is not valid for this…
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Class II · 10 months ago
ICU Medical, Inc. LifeShield Drug Library Management recall: For certain customers, the Change Summary review option ceases to operate
For certain customers, the Change Summary review option ceases to operate as expected for any migrated library after the migration has been…
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Class II · 10 months ago
Zimmer, Inc. Brand Name: Affixus Antegrade Femoral Nailing System Product Name recall: Affected implants may have undersized distal diameter along length
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk…
-
Class II · 10 months ago
Zimmer, Inc. Brand Name: Affixus Antegrade Femoral Nailing System Product Name recall: Affected implants may have undersized distal diameter along length
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk…
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Class II · 10 months ago
Medtronic Neuromodulation Restore Clinician Programmer Application recall: Software issue where a Device Reset message displayed on the app was unable
Software issue where a Device Reset message displayed on the app was unable to be cleared. In rare cases, this resulted in an inability to resume…
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Class II · 10 months ago
CareFusion 303, Inc. BD Pyxis MedStation ES, REF: 323, BD Pyxis MedStation ES 7 Drawer recall: Automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer
Automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer firmware update, which caused a Cubie Insert event which prompts software to…
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Class II · 10 months ago
Merck Sharp & Dohme LLC Noxafil Powdermix for Delayed-Release Oral Suspension, 300 mg recall: Presence of particulate matter: potential presence of metal particulates
Presence of particulate matter: potential presence of metal particulates in the product.
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Class II · 10 months ago
Merck Emend for oral suspension, 125 mg, Single-Dose Kit recall: Presence of particulate matter: potential presence of metal particulates
Presence of particulate matter: potential presence of metal particulates in the product.
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Class I · 10 months ago
Carousel Candies Choceur Cookie Butter Holiday Bark. Standup Pouch Bag. 5 oz recall: Undeclared pecan
Undeclared pecan
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Class I · 10 months ago
Carousel Candies Choceur Pecan Cranberry & Cinnamon Holiday Bark. Standup Pouch Bag recall: Undeclared wheat
Undeclared wheat
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Class II · 10 months ago
Chips Ahoy Baked brownie bites recall: Product Safety – choking threats
Product Safety – choking threats
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Class II · 10 months ago
Gold Star Distribution All FDA-regulated products held at facility including drugs recall: Potential Salmonella contamination, presence of rodent and avian
Potential Salmonella contamination, presence of rodent and avian contamination and insanitary conditions during the storage process.