Latest recalls — page 84
Older notices, newest first.
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Class II · 4 months ago
Medline Medical Procedure Kits labeled as: Pelvic LAP 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
Medline convenience kits: Davinci Dynj905836D Davinci-Lf Dynj905293I 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
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
Abiomed, Inc. Impella CP Set with SmartAssist. Product Codes: 1000080 recall: Exposure to the low purge pressure occurrence may result in persistent low
Exposure to the low purge pressure occurrence may result in persistent low purge pressure alarms and, in some cases, interruption or loss of…
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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.