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Abbott Laboratories Inc.

Abbott Laboratories Inc. Recalls

All product recalls associated with Abbott Laboratories Inc..

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

143

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 33801–33820 of 37665 recalls

Abbott Laboratories Inc.: MULTIGENT Acetaminophen, List Number 2K99-20

Lipase results are falsely elevated when a MULTIGENT Acetaminophen test is pipetted immediately before a Lipase test from the same sample cup or tube on the ARCHITECT c8000.

FDAJun 1, 2007PR• Abbott Laboratories Inc.

The Sisus Corporation: Non-AC-powererd Patient Lifts for assisting patients whe...

Poor welding may cause the device(s) to fail, which may result in the user, falling in the bathroom and/or a lack of assistance with bathing or toileting.

FDAJun 1, 2007Nationwide• The Sisus Corporation

Quantimetrix Corporation: Quantimetrix Dip and Spin Control Urine Dipstick/Microsco...

This recall was initiated due to efficacy concerns with the stabilized erythrocytes, leukocytes and lymphocytes contained in this product group.

FDA

1...1689 169016911692 1693...1884

Page 1691 of 1884Next

Jun 1, 2007

Nationwide

• Quantimetrix Corporation

Abbott Laboratories Inc.: Clinical Chemistry Lipase, List Numbers: 7D80-20 and 7D80-30

Lipase results are falsely elevated when a MULTIGENT Acetaminophen test is pipetted immediately before a Lipase test from the same sample cup or tube on the ARCHITECT c8000.

FDAJun 1, 2007PR• Abbott Laboratories Inc.

Quantimetrix Corporation: Quantimetrix Synovialscopics Synovial Fluid Control. Sy...

This recall was initiated due to efficacy concerns with the stabilized erythrocytes, leukocytes and lymphocytes contained in this product group.

FDAJun 1, 2007Nationwide• Quantimetrix Corporation

Abbott Diagnostic International, Ltd. 30 Bo Cruce Davila: XSYSTEMS Quinidine Controls are composed of 3 bottles of ...

Controls Out of Range/Specification.

FDAMay 31, 2007AZ, AR, CA +29 more• Abbott Diagnostic International, Ltd. 30 Bo Cruce Davila

Abbott Diagnostic International, Ltd. 30 Bo Cruce Davila: AxSYM Quinidine Controls - are composed of 3 bottles of c...

Controls Out of Range/Specification .

FDAMay 31, 2007AZ, AR, CA +29 more• Abbott Diagnostic International, Ltd. 30 Bo Cruce Davila

Abbott Diagnostic International, Ltd. 30 Bo Cruce Davila: XSYSTEMS Quinidine Calibrators consists of six bottles of...

Controls Out of Range/Specification.

FDAMay 31, 2007AZ, AR, CA +29 more• Abbott Diagnostic International, Ltd. 30 Bo Cruce Davila

Abbott Diagnostic International, Ltd. 30 Bo Cruce Davila: AxSYM Quinidine Standard Calibrators - consist of six bot...

Controls Out of Range/Specification .

FDAMay 31, 2007AZ, AR, CA +29 more• Abbott Diagnostic International, Ltd. 30 Bo Cruce Davila

Polaris Hawkeye ATVs – steering failure (2007)

Only certain model year 2006 Polaris Hawkeye ATVs produced prior to January 23, 2006 are included in this recall. Consumers should contact Polaris to identify whether their model is part of the recall. All serial number ranges of the Hawkeye 2x4 model number A06LB27AA and the Hawkeye 4x4 model number A06LD27AA/AB/AC are included. The serial number (VIN) identification decal is located under the right-hand front fender and stamped on the lower portion of the frame, behind the left front wheel.

CPSCMay 30, 2007Nationwide• Polaris Industries Inc., of Medina, Minn.

Stryker Howmedica Osteonics Corp.: Trident Hemispherical Acetabular Shell; 72mm, Arc Deposit...

Stryker Orthopaedics became aware that Trident Hemispherical Shells, Catalog Number 508-11-74J, are actually marked and labeled as Catalog Number 598-11-72J, Lot Code 20282301

FDAMay 29, 2007Nationwide• Stryker Howmedica Osteonics Corp.

Philips Medical Systems (Cleveland) Inc: Brilliance CT Systems 64 slice configuration. Computed to...

Two potential artifacts may appear in some images from head scans on the Brilliance 40/64 systems. These artifacts may lead to misdiagnosis.

FDAMay 25, 2007PR• Philips Medical Systems (Cleveland) Inc

Philips Medical Systems (Cleveland) Inc: Brilliance CT Systems, 40 slice configuration. Computed ...

Two potential artifacts may appear in some images from head scans on the Brilliance 40/64 systems. These artifacts may lead to misdiagnosis.

FDAMay 25, 2007PR• Philips Medical Systems (Cleveland) Inc

OEC Medical Systems, Inc: OEC Miniview 6800 mobile fluoroscopic x-ray system, GE He...

X-ray systems did not have the required labeling to indicate Air Kerma Rate and cumulative Air Kerma during fluoroscopic procedures

FDAMay 24, 2007AK, CA, CO +16 more• OEC Medical Systems, Inc

Invincibles Transport Converters (Toy Century) – Lead Poisoning Risk (2007)

This recall involves toy sets with multiple action figures and vehicles. The model number (88931), Universal Product Code (6 98567 88931 4) and Soldier Bear logo are printed on the product's packaging. The backs of the action figures are marked with letters "TC-ST."

CPSCMay 23, 2007Nationwide• Toy Century Industrial Ltd., of Hong Kong

Terumo Cardiovascular Systems Corp: Terumo TenderFlow Pediatric Arterial Cannulae, 2.0 mm (6F...

The bond may fail and a leak or separation of the device occur at the distal end (where this device connects to the arterial line).

FDAMay 22, 2007Nationwide• Terumo Cardiovascular Systems Corp

Beckman Coulter Inc: Beckman Coulter Flow-Count Fluorospheres - Part Number 75...

Sporadic absolute count recovery failures with assayed control cell products when using Lot Number 754801F of the Flow-Count Fluorospheres. Additionally, this lot has experienced secondary fluorescent populations containing more than 20% of the total population, as stated in the Evidence of Deterioration section of the Package Insert.

FDAMay 21, 2007Nationwide• Beckman Coulter Inc

Roche Molecular Systems, Inc.: Amplilink Software versions 1.1, 1.3, 1.4, 2.41. COBAS Am...

For select COBAS AMPLICOR Tests run on the COBAS AMPLICOR Analyzer in conjunction with AMPLILINK software, a discrepancy has been identified between the onboard working reagent stability information reported by AMPLILINK Software (versions 1.1, 1.3, 1.4 and 2.41) and the stability information provided in the test kit package inserts/method manual.

FDAMay 21, 2007Nationwide• Roche Molecular Systems, Inc.

The Anspach Effort, Inc.: Anspach Single Use, Sterile Bone Cutting Burrs

The white film portion of the sterile pouch may become brittle prior to the expiry date compromising the sterility of the product.

FDAMay 18, 2007Nationwide• The Anspach Effort, Inc.

Kentec Medical Inc: Reusable Ohmeda Compatible Finger Clip Sensor, Model Numb...

Incompatible components: The Finger Clip Sensors - with a Serial Number prefix of PA514, PA515, YE508, ZC502 and ZG512 - are missing an additional diode and higher resistor in its existing configuration making them inoperable when used to interface with those Ohmeda Tuffsat monitors previously re-configured by Ohmeda to include a detection circuit for diodes.

FDAMay 18, 2007Nationwide• Kentec Medical Inc