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All product recalls associated with Datascope Corp.
Total Recalls
1000
Past Year
1000
Class I (Serious)
145
Most Recent
Jan 2026
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
10.5 Fr. Percor STAT-DL Intra-Aortic Balloon Insertion Kit, Introducer Sheath failed water leak test during final inspection.
Tandem Hemodialysis Catheter may have splits in the catheter shaft below the extension adapter
The defective device may restrict the flow of sterilant to the attached endoscope and affect the sterilization process of the scope.
Label lacks professional use legend and name and address of the manufacturer.
Lacks professional use labeling and firm name and address.
Label lacks professional use legend and name and address of the manufacturer.
The dialysis treatment may be run without the bicarbonate due to an undetected bicarbonate pump stall following a sodium change.
Label lacks professional use legend and name and address of the manufacturer.
Label lacks professional use legend and name and address of the manufacturer.
The outer labeling of the convenience kit indicates that an additional bottle of Sodium Chloride (saline) solution is included in the Custom Kit 31176; however, an additional bottle of 1% Xylocaine was included in the Custom Kit.
Abnormal results are flagged as normal.
Knee frame defect lead to breakage and injury. Knee bolt end came loose.
Warning flag may be detached from the tip protector on the catheter and result in the tip protector advancing through the catheter during use
A software error could have resulted in the delivery of a larger bolus of insulin than anticipated when the pump was programmed in a particular manner.
The 6-ounce red Christmas candles are packaged in an 18-count box labeled "Christmas Candles." Each candle sits in a 6-ounce tin container. A label on the bottom of the candle reads in part, "Merry Christmas" with either a Santa Claus or Christmas tree printed on the candle. The candles have a cinnamon spice fragrance named Christmas Joy. Only the 6-ounce candle size is included in the recall.
The recalled engines are 27-horsepower, liquid-cooled, overhead-valve (OHV), V-twin models with electric start and horizontal output shafts. The engine model and serial numbers are on a label at the top of the engines and next to the radiator cap: Engine Model Application Specification Engine Serial No. FD750D AS02 000001 through 020851
The recalled power supplies are used with notification appliance circuits that provide an audible, visual, or audio-visual combination notification to building occupants in the event of a fire. Only power supplies with a date code of 4602 or lower are included in this recall.
The needle portion of the Safety Blood Collection Sets, may become separated from the body of the Luer Adapter.
The Steris device may not attach properly to retrofitted Olympus bronchoscopes, and become loose during the sterile processing cycle.
Incorrect bar code applied to cartridges could result in inaccurate pO2 value