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Abbott Diagnostic International, Ltd. 30 Bo Cruce Davila

Abbott Diagnostic International, Ltd. 30 Bo Cruce Davila Recalls

All product recalls associated with Abbott Diagnostic International, Ltd. 30 Bo Cruce Davila.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

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.

Showing 18781–18800 of 21319 recalls

Abbott Diagnostic International, Ltd. 30 Bo Cruce Davila: Abbott AxSYM System Digoxin III Reagent Pack

Customers are receiving error codes (1062, 1063, 1113, & 1118) when running patient samples on the AxSYM Digoxin III assay.

FDAMar 30, 2007PR• Abbott Diagnostic International, Ltd. 30 Bo Cruce Davila

Siemens Medical Solutions USA, Inc: Magnetom Espree System with OR Table

If table top is not seated properly it can lock up/stick.

FDAMar 30, 2007IN, NY, TX• Siemens Medical Solutions USA, Inc

Medtronic Emergency Response Systems, Inc.: LIFEPAK 20 defibrillator/monitor. The device is an AC po...

Defibrillator internal battery cell may contain a short which could reduce battery capacity and cause the device to shut down without warning while operating on backup (DC) battery power.

FDAMar 30, 2007

1...938 939940941 942...1066

Page 940 of 1066Next

• Medtronic Emergency Response Systems, Inc.

Diagnostica Stago, Inc.: STA Neoplastine CI Plus (10), (cat. 0667). 12 x 10 ml. i...

Based on the confirmed clotting times in the upper part of the assigned ranges of STA-Coag Control ABN control plasmas when used with STA-Neoplastine CI Plus, use of this lot may cause difficulty during the validation of the STA-Coag Control ABN.

FDAMar 30, 2007Nationwide• Diagnostica Stago, Inc.

Electric Mobility Corp: Rascal Scooters with Electric seat lifts, Model 600 Serie...

Seat and/or lift actuator problems: 1) Models equipped with a Seat Lift, the mast screw and washer holding the Seat Lift Actuator in place will loosen break off or fall out; 2) Models assembled with Seat Lift Actuator or Seat Post Mounting Bolts, the seat may wobble or the seat will break off from the vehicle; 3) Models using Seat-On Lifting brackets with a hoist to raise an EMC vehicle equipped w

FDAMar 29, 2007Nationwide• Electric Mobility Corp

Triax PK7 Bicycles (Shun Lu) – Frame Failure (2007)

This recall involves Triax PK7 (model 8509-24) and Vertical PK7 (model 8596-71T) 20-inch aluminum cushion framed bicycles. The Triax model was manufactured between November 2005 and October 2006, and the Vertical model was manufactured between August 2004 and December 2004. The model numbers and manufacture dates are printed on a label affixed to the bicycle frame.

CPSCMar 28, 2007Nationwide• Shun Lu Bicycle Company, of Guangdong, China

GE OEC Medical Systems, Inc: OEC MiniView 6800 Mobile; MDL number A349855. Product ...

Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being classified by the Agency. GE OEC had discovered an issue with the hard disk drives that were installed on OEC device models: UroView 2800; 9800 Plus Digital; MiniView 6800; and FlexiView 8800 Mobile C-Arm. The devices were manufactured between October 15, 2004 and

Class IIModerate

FDAMar 27, 2007Nationwide• GE OEC Medical Systems, Inc

Wright Medical Technology Inc: Profemur R, Revision Hip system, Proximal Body (part), X-...

The titanium plasma coating was found to have missing fragments.

FDAMar 27, 2007Nationwide• Wright Medical Technology Inc

Sendx Medical Inc: ABL80 FLEX Analyzer, Model #393-839

There have been reported experiences where waste fluids have sprayed out from the waste drain at the front of the ABL80 analyzer when excessive pressure builds within the waste line.

FDAMar 27, 2007OH• Sendx Medical Inc

GE OEC Medical Systems, Inc: OEC 9800 Plus Digital; MDL number A349855. Product Usage...

FDAMar 27, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: UroView 2800; MDL number A349855. Product Usage: Designe...

FDAMar 27, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC 9800 Plus Digital; MDL number A349855. Product Usa...

Class IIModerate

FDAMar 27, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: UroView 2800; MDL number A349855. Product Usage: Desig...

Class IIModerate

FDAMar 27, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC MiniView 6800 Mobile; MDL number A349855. Product Us...

FDAMar 27, 2007Nationwide• GE OEC Medical Systems, Inc

General Electric Med Systems LLC: GE Healthcare Innova 3100/ 3100 IQ Digital Fluoroscopic ...

Caution on the non-detection of small invasive objects/devices, which project out from the skin surfaces (e.g. biopsy or other needles) while using the Innova Sense software option designed for patient contouring. Usage of Innova Sense patient contouring for such devices could potentially lead to patient injury.

FDAMar 26, 2007Nationwide• General Electric Med Systems LLC

General Electric Med Systems LLC: GE Healthcare Innova 4100/4100 IQ. Digital Fluoroscopic ...

Measurement errors during the computation of vessel diameters while using the Stenosis Analysis software (also known as Quantitative Coronary Analysis function-QCA) using the auto-calibration function on Innova Digital (located in control room) or in-room InnovaCentral/Touch-Screen

FDAMar 26, 2007AZ, CA, CO +22 more• General Electric Med Systems LLC

General Electric Med Systems LLC: GE Healthcare Innova 2100 IQ Digital Fluoroscopic Imaging...

FDAMar 26, 2007Nationwide• General Electric Med Systems LLC

General Electric Med Systems LLC: GE Healthcare Innova 3100/ 3100 IQ Digital Fluoroscopic...

FDAMar 26, 2007AZ, CA, CO +22 more• General Electric Med Systems LLC

General Electric Med Systems LLC: GE Healthcare Innova 2100 IQ Digital Fluoroscopic Imagin...

FDAMar 26, 2007AZ, CA, CO +22 more• General Electric Med Systems LLC

Philips Medical Systems North America Co. Phillips: Practix 160 Mobile X-ray systems. The systems are used i...

X-ray systems lack product report certification demonstrating compliance, and were illegally introduced into the United States commerce.

FDAMar 23, 2007Nationwide• Philips Medical Systems North America Co. Phillips