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Medical Devices Recalls

Medical equipment, implants, and diagnostic devices

38,779 Total Recalls

Ortho Clinical Diagnostics issued a Product Correction Notification for VITROS Immunodiagnostic Products CA 125 II Reagent Pack and Calibrators due to a positive shift in patient results.

Oct 9, 2013 Diagnostic Equipment Nationwide View Details →

Products were shipped labeled with "use by" dates that exceed currently available shelf-life data. All products remain within the earliest expiration date of April 2015.

Nov 4, 2013 Diagnostic Equipment Nationwide View Details →

KARL STORZ Endoscopy America, Inc. is recalling the Flexible Broncho Fiberscope or a Flexible Intubation Fiberscope with a suction port because the material used in the suction channel portion was thermoplastic polyurethane (TPU), which is not listed in STERRAD systems claims for interior endoscope lumens.

Nov 13, 2013 Other Medical Devices Nationwide View Details →

This issue is only relevant for customers importing xml files into the MagNA Pure 96 IVD instrument software for sample identification. There is a potential for sample mismatch when using the MagNA Pure 96 IVD instrument (catalog number 06541089001). Importing an order file in xml format to the MagNA Pure 96 IVD instrument software may result in a wrong sequence of samples in the graphical overvi

Nov 25, 2013 Other Medical Devices View Details →

Products were shipped labeled with "use by" dates that exceed currently available shelf-life data. All products remain within the earliest expiration date of April 2015.

Nov 4, 2013 Diagnostic Equipment Nationwide View Details →

Products were shipped labeled with "use by" dates that exceed currently available shelf-life data. All products remain within the earliest expiration date of April 2015.

Nov 4, 2013 Diagnostic Equipment Nationwide View Details →

The product may give weak or false negative test results.

May 2, 2013 Diagnostic Equipment Nationwide View Details →

Qualigen initiated this recall because the FastPack kit may cause lower than expected results due to a manufacturing defect.

Nov 8, 2013 Infusion Pumps View Details →

Products were shipped labeled with "use by" dates that exceed currently available shelf-life data. All products remain within the earliest expiration date of April 2015.

Nov 4, 2013 Diagnostic Equipment Nationwide View Details →

Qualigen initiated this recall because the FastPack kit may cause lower than expected results due to a manufacturing defect.

Nov 8, 2013 Infusion Pumps View Details →

Promotional materials for non-medical water filtration products were determined to promote claims which constitute marketing the product as a medical device.

Oct 28, 2013 Infusion Pumps Nationwide View Details →

Products were shipped labeled with "use by" dates that exceed currently available shelf-life data. All products remain within the earliest expiration date of April 2015.

Nov 4, 2013 Diagnostic Equipment Nationwide View Details →

Products were shipped labeled with "use by" dates that exceed currently available shelf-life data. All products remain within the earliest expiration date of April 2015.

Nov 4, 2013 Diagnostic Equipment Nationwide View Details →

Products were shipped labeled with "use by" dates that exceed currently available shelf-life data. All products remain within the earliest expiration date of April 2015.

Nov 4, 2013 Diagnostic Equipment Nationwide View Details →

Products were shipped labeled with "use by" dates that exceed currently available shelf-life data. All products remain within the earliest expiration date of April 2015.

Nov 4, 2013 Diagnostic Equipment Nationwide View Details →

Baxter Healthcare Corporation is issuing a voluntary correction for ABACUS Total parenteral Nutrition (TPN) Calculation Software versions 2.0 through 3.0 due to the possibility that a patient could receive another patient's TPN order as a result of data corruption.

Dec 3, 2013 Infusion Pumps Nationwide View Details →

Products were shipped labeled with "use by" dates that exceed currently available shelf-life data. All products remain within the earliest expiration date of April 2015.

Nov 4, 2013 Diagnostic Equipment Nationwide View Details →

Firm has become aware of the potential for detachment of the jaw insert for Large Needle Drivers and Mega Needle Drivers.

Nov 15, 2013 Surgical Instruments Nationwide View Details →