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Abbott Laboratories HPD/ADD/GPRD

Abbott Laboratories HPD/ADD/GPRD Recalls

All product recalls associated with Abbott Laboratories HPD/ADD/GPRD.

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Recall Summary

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.

Showing 36761–36780 of 37661 recalls

Abbott Laboratories HPD/ADD/GPRD: IMx Rubella IgM Reagent Kit, 100 tests, list 7A24-20; Abb...

The package insert contains incomplete information for the English text. Pages 4 and 5 are missing and pages 14 and 15 are duplicated.

FDAJul 22, 2003CA, GA, IL +8 more• Abbott Laboratories HPD/ADD/GPRD

Misys Healthcare Systems: Misys Laboratory System versions 5.2 through 5.3.2 using ...

Software design deficiency. If the dilution factor is added to the same result twice, incorrect specimen values are reported.

FDAJul 22, 2003Nationwide• Misys Healthcare Systems

Abbott Vascular Devices: BiodivYsio SV Over The Wire (OTW) Coronary Stent, 2.25 mm...

The medical device is misbranded in that the compliance chart of the Stent diameter may allow overexpansion that may result in vessel damage.

FDA

1...1837 183818391840 1841...1884

Page 1839 of 1884Next

Jul 21, 2003

Nationwide

• Abbott Vascular Devices

Misys Healthcare Systems: Misys Laboratory System, versions 5.3 build 63 through 5....

Incorrect demographics display which can result in incorrect information being used in diagnosis or treatment of patients.

FDAJul 21, 2003Nationwide• Misys Healthcare Systems

Alcon Laboratories, Inc.: ''Alcon Ladarwave CustomCornea Wavefront System'' Aberrom...

Software error could, under specific circumstances, allow the patient's centration images and data to be stored incorrectly.

FDAJul 21, 2003Nationwide• Alcon Laboratories, Inc.

Philips Medical Systems Sales & Service Region No. America: Diagnost 97

Labeling of push button caps located on the control panel may not clearly identify the applied Source to Image distance (SID).

FDAJul 17, 2003Nationwide• Philips Medical Systems Sales & Service Region No. America

Philips Medical Systems Sales & Service Region No. America: OmniDiagnost System

Labeling of push button caps located on the control panel may not clearly identify the applied Source to Image distance (SID).

FDAJul 17, 2003Nationwide• Philips Medical Systems Sales & Service Region No. America

Stryker Howmedica Osteonics: Femoral Resection Guide, Scorpio L.R.S. Instrumentation.

Scorpio Femoral Resection Guides have the potential to remove more bone than necessary.

FDAJul 17, 2003IN• Stryker Howmedica Osteonics

Oil Lamp Boxed Sets (DesignPac) – Flammability Risk (2003)

The boxed sets contain a clear vase with pink or purple floral designs, and a 16-ounce bottle of paraffin oil. The packaging is labeled "Handpainted Oil Lamp Set" and "Floral Garden." Item number 054 11 0229 is printed on the packaging.

CPSCJul 17, 2003Nationwide• DesignPac, of Northlake, Ill.

Novelty Cigarette Lighters (De Bon Sales) – Design Hazard (2003)

Fire/Burn Risk

There are two styles of lighters included in this recall. The first is a chrome and silver lighter, in the shape of a rearing horse. It is about 2.3 inches long and is labeled "DE-L-36." The second lighter is silver-colored, in the shape of a bird head holding a snake. It is about 2.5 inches long and is labeled "DE-L-23."

CPSCJul 17, 2003Nationwide• De Bon Sales Inc., of Houston, Texas

Slow Cookers (Hamilton Beach) – Electrical Safety Risk (2003)

Fire/Burn Risk

The recalled slow cookers were sold under the Hamilton Beach and Proctor-Silex brand names, which are printed on the front of the base of the unit. The slow cookers are either round or oval, and were sold in solid white and various print designs. They have a capacity of 3.5 to 6.5 quarts. The slow cookers have series codes A through D which are printed on the bottom along with the model number. Brand Names Model Numbers Hamilton Beach 33390, 33475, 33575, 33590, 33675, 33690, 33725, 33850, 33860 Hamilton Beach / Portfolio 33680 Proctor-Silex 33320, 33320FD, 33325, 33375, 33380, 33625A

CPSCJul 17, 2003Nationwide• Hamilton Beach/Proctor-Silex, of Glen Allen, Va.

Smart Dive Computers (UWATEC) – Potential Malfunction (2003)

The recalled units are the UWATEC Smart PRO and the Smart COM dive computers. The Smart PRO is offered as a console and as a wrist unit. The Smart COM only comes in a console model. The names of each unit appear on the computer case, along with the name "UWATEC."

CPSCJul 17, 2003Nationwide• UWATEC AG, of Hallwil, Switzerland