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Abbott Laboratories

Abbott Laboratories Recalls

All product recalls associated with Abbott Laboratories.

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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 31801–31820 of 37665 recalls

CELL-DYN 1800 (Abbott) - Syringe Leakage Risk (2009)

Use of Syringe LN 04H36-01 with the Die-cast syringe drive may result in leakage, leading to delay in reporting patient results.

FDAJun 8, 2009Nationwide• Abbott Laboratories

CELL-DYNE 1700CS (Abbott) - Syringe Leakage Risk (2009)

Use of Syringe LN 04H36-01 with the Die-cast syringe drive may result in leakage, leading to delay in reporting patient results.

FDAJun 8, 2009Nationwide• Abbott Laboratories

CELL-DYN 1700 (Abbott) - Syringe Leakage Risk (2009)

Use of Syringe LN 04H36-01 with the Die-cast syringe drive may result in leakage, leading to delay in reporting patient results.

FDAJun 8, 2009Nationwide• Abbott Laboratories

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Prosthesis Knee (Endotec) - Sterility Issues (2009)

Endotec is recalling B-P Hip, B-P Shoulder, and B-P Knee Replacement System devices due to sterility issues involving validation, process variations and test results.

FDAJun 5, 2009CA, FL, IN +4 more• Endotec, Inc.

Exogen 4000+ Bone Healing System (Smith & Nephew) - Transducer Problem (2009)

Problems with transducer may result in a reduced ultrasound output.

FDAJun 5, 2009Nationwide• Smith & Nephew Inc

Prosthesis Ankle (Endotec) - Sterility Issues (2009)

Endotec is recalling B-P Hip, B-P Shoulder, and B-P Knee Replacement System devices due to sterility issues involving validation, process variations and test results.

FDAJun 5, 2009CA, FL, IN +4 more• Endotec, Inc.

PTS Lipids Panel Strips (Polymer Technology) - Under-Recovery (2009)

Exhibits under-recovery of all analytes.

FDAJun 5, 2009Nationwide• Polymer Technology Systems, Inc.

Exogen Express Bone Healing System (Smith & Nephew) - Transducer Problem (2009)

Problems with transducer may result in a reduced ultrasound output.

FDAJun 5, 2009Nationwide• Smith & Nephew Inc

Prosthesis Hip (Endotec) - Sterility Issues (2009)

Endotec is recalling B-P Hip, B-P Shoulder, and B-P Knee Replacement System devices due to sterility issues involving validation, process variations and test results.

FDAJun 5, 2009CA, FL, IN +4 more• Endotec, Inc.

Uni-Circuit Kit (GE Healthcare) - Tube Separation Risk (2009)

Breathing circuit inner tube may separate from the rigid connectors under certain conditions. A separation of the inner tube from the connector may prevent adequate gas flow (O2, N2O and anesthetic agents) to the patient. A separation can also cause CO2 re-breathing. This could lead to hypoxia and/or hypercarbia and inadequate anesthesia delivery.

FDAJun 5, 2009Nationwide• GE Medical Systems, LLC

Prosthesis Shoulder (Endotec) - Sterility Issues (2009)

Endotec is recalling B-P Hip, B-P Shoulder, and B-P Knee Replacement System devices due to sterility issues involving validation, process variations and test results.

FDAJun 5, 2009CA, FL, IN +4 more• Endotec, Inc.

TMJ Components (Endotec) - Sterility Issues (2009)

Endotec is recalling B-P Hip, B-P Shoulder, and B-P Knee Replacement System devices due to sterility issues involving validation, process variations and test results.

FDAJun 5, 2009CA, FL, IN +4 more• Endotec, Inc.

Apelo Modular Screwdriver (Atlas Spine) - Complaint Received (2009)

Atlas Spine, Inc. recalled their Apelo Modular Screwdriver, a component of the Apelo Pedicle Screw System Instrumentation, because of complaints received about the tip breaking. If the tip is fractured inside of the modular screw, the tip could become implanted in the body or if the entire screw is removed, it could cause a delay in the surgery.

FDAJun 4, 2009FL• Atlas Spine, Inc.

Apelo Modular Screwdriver (Atlas Spine) - Complaint Received (2009)

Class IIModerate

FDAJun 4, 2009FL• Atlas Spine, Inc.

Mueller-Hinton Broth (Trek Diagnostics) - Unapproved Shipment (2009)

Thirty-one boxes of unapproved quarantine product, CP112-10 MHB w/LHB, Lot # 150444SA, were inadvertently shipped to customers on 6/2/09 instead of shipping approved Lot # 150344SA.

FDAJun 4, 2009Nationwide• Trek Diagnostic Systems

Microm STP 420D Tissue Processor (Thermo Fisher) - Performance Issues (2009)

The firm has received complaints regarding specimen integrity (higher rate of specimen fragmentation) as well as complaints that the chamber may stop rotating prematurely, resulting in sample deterioration.

FDAJun 3, 2009HI, KY, LA +11 more• Thermo Fisher Scientific

Bigger Better-Bladder (Circulatory Technology) - Silent Recall (2009)

During an FDA inspection, it was discovered that the firm had conducted a silent recall of its Bigger Better Bladder device after receiving a complaint from a hospital that the device collapsed during a procedure thereby obstructing flow.

FDAJun 3, 2009AZ, AR, CA +14 more• Circulatory Technology Inc

Rapid Programmer Software (Advanced Neuromodulation) - Unapproved Version (2009)

Product programmed with unapproved software was distributed.

FDAJun 2, 2009IN, NH, PR• Advanced Neuromodulation Systems

Bee Strollers (Bugaboo) – brake failure (2009)

Bugaboo Bee strollers have item code 580210 on a label on the back of the seat and item code 50100 on a label on the plastic support under the seat. The strollers were sold in blue, dark khaki, pink, red, yellow, and black. "bugaboo® bee" is printed on the left side of the seat.

CPSCJun 2, 2009Nationwide• Bugaboo Design & Sales, B.V., of the Netherlands

AMPLILINK Software (Roche Molecular) - Software Bug (2009)

Software bug: A unique series of events involving the COBAS AmpliPrep instrument running AMPLILINK software version 3.2.2 that results in specimens being amplified and detected with the wrong parameters. The error can occur on either COBAS AmpliPrep/COBAS TaqMan 48, COBAS AmpliPrep/COBAS TaqMan (docked) or cobas s 201 system (docked) running Amplilink Software versions 3.1 or 3.2 series up to and

FDAJun 2, 2009Nationwide• Roche Molecular Systems, Inc.