Recalls affecting West Virginia
Notices that name West Virginia in their distribution area, plus every nationwide recall — nationwide recalls reach West Virginia too.
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Class II · 4 months ago
ConMed AirSeal 12mm Access Port and Low Profile Obturator recall: Potential for overpressure alerts
Potential for overpressure alerts.
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Class I · 4 months ago
Arrow International, LLC Description/REF: PI Agba Picc KIT: 3L 6 FR X 40 CM recall: Lidocaine, Bupivacaine, and 0.9% sodium chloride
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have…
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Class I · 4 months ago
Arrow International, LLC Description/REF: Arterial Line KIT: SL 20 GA X 5 recall: Lidocaine, Bupivacaine, and 0.9% sodium chloride
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have…
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Class II · 4 months ago
ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless recall: Potential for overpressure alerts
Potential for overpressure alerts.
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Class II · 4 months ago
Thoratec LLC Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System recall: Due to 11 volt Backup Battery failures
Due to 11 volt Backup Battery failures.
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Class II · 4 months ago
ConMed AirSeal 12mm Access Port and Obturator with Blunt Tip recall: Potential for overpressure alerts
Potential for overpressure alerts.
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Class I · 4 months ago
Arrow International, LLC Description/REF: Paracentesis KIT/ASK-00376-JHH recall: Lidocaine, Bupivacaine, and 0.9% sodium chloride
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have…
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Class II · 4 months ago
Medline convenience kits: ACD Dynj904999J Acdf Dynj907336B Dynj910821A recall: Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable…
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Class II · 4 months ago
Thoratec LLC Brand Name: HeartMate Product Name: HeartMate 3" System Controller recall: Due to 11 volt Backup Battery failures
Due to 11 volt Backup Battery failures.
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Class II · 4 months ago
Medline convenience kits: Davinci Main Dynj908031D recall: Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable…
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Class I · 4 months ago
Arrow International, LLC Description/REF: Access Tray/GU-04020 recall: Lidocaine, Bupivacaine, and 0.9% sodium chloride
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have…
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Class II · 4 months ago
Medline Medical Procedure Kits labeled as: Laparoscopy Combined recall: During an internal review, Medline identified representative samples did
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include…
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Class I · 4 months ago
Arrow International, LLC Description/REF: Hemodialysis KIT: 2-Lumen 12 FR X 20 recall: Lidocaine, Bupivacaine, and 0.9% sodium chloride
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have…
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Class II · 4 months ago
Medline convenience kits: CMH Central Line Dressing Change KIT recall: Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable…
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Class II · 4 months ago
Howmedica Osteonics Corp. TRI TS Baseplate Size 3 recall: Stryker has identified that Triathlon Universal Baseplate Size 3 (lot
Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate…
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Class I · 4 months ago
Arrow International, LLC Description/REF: Epidural Catheter KIT: 19 GA X 90 recall: Lidocaine, Bupivacaine, and 0.9% sodium chloride
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have…
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Class I · 4 months ago
Arrow International, LLC Description/REF: PI Jacc KIT: 2L 5.5 FR X 15 CM recall: Lidocaine, Bupivacaine, and 0.9% sodium chloride
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have…
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Class II · 4 months ago
Medline Medical Procedure Kits labeled as CH Open Heart recall: During an internal review, Medline identified representative samples did
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include…
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Class II · 4 months ago
Medline Medical Procedure Kits labeled as: 1) CV Draping/Basin recall: During an internal review, Medline identified representative samples did
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include…
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Class II · 4 months ago
Brand Name: Inspire Medical Systems, Inc. Product Name: Inspire recall: Products are labeled with incorrect Use By Date
Products are labeled with incorrect Use By Date, extending beyond the validated three-year shelf life from date of manufacturer. Material degradation…
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Class II · 4 months ago
Medtronic O-arm O2 Imaging System recall: Potential for image artifacts caused by an anomaly in the O-arm O2 Imaging
Potential for image artifacts caused by an anomaly in the O-arm O2 Imaging System s detector panel firmware.
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Class II · 4 months ago
Medline Medical Procedure Kits labeled as: 1) Basic Heart Pack recall: During an internal review, Medline identified representative samples did
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include…
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Class II · 4 months ago
Dabur India Limited Med Pride, Bacitracin Zinc Ointment, 500 units, 0.9g packets recall: CGMP Deviations; deficiencies observed during FDA inspection
CGMP Deviations; deficiencies observed during FDA inspection
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Class II · 4 months ago
Dabur India Limited Cura Hongos, Crema Antifungica, Clotrimazole 1%, 2oz tubes recall: CGMP Deviations; deficiencies observed during FDA inspection
CGMP Deviations; deficiencies observed during FDA inspection