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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

295

Class I (Serious)

116

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 3801–3820 of 4465 recalls

Abbott Laboratories: AxSYM HBsAg Reagent Pack; Abbott Laboratories, Abbott Par...

Defective caps: Customers have observed reagent bottles not opening appropriately, which could lead to a probe crash on the instrument.

FDAJan 19, 2009PR• Abbott Laboratories

Abbott Laboratories: AxSYM Troponin-I ADV Reagent Pack, Abbott Laboratories, A...

Defective caps: Customers have observed reagent bottles not opening appropriately, which could lead to a probe crash on the instrument.

FDAJan 19, 2009PR• Abbott Laboratories

Abbott Laboratories: AxSYM Folate Reagent Pack; Abbott Laboratories, Abbott P...

Defective caps: Customers have observed reagent bottles not opening appropriately, which could lead to a probe crash on the instrument.

FDAJan 19, 2009PR• Abbott Laboratories

1...189 190191192 193...224

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Abbott Laboratories: AxSYM CMV IgG Reagent Pack; Abbott Laboratories, Abbott P...

Defective caps: Customers have observed reagent bottles not opening appropriately, which could lead to a probe crash on the instrument.

FDAJan 19, 2009PR• Abbott Laboratories

Abbott Laboratories: AxSYM CORE 2.0 Reagent Pack; Abbott Laboratories, Abbott ...

Defective caps: Customers have observed reagent bottles not opening appropriately, which could lead to a probe crash on the instrument.

FDAJan 19, 2009PR• Abbott Laboratories

Abbott Laboratories: AxSYM Myoglobin Reagent Pack, Abbott Laboratories, Abbott...

Defective caps: Customers have observed reagent bottles not opening appropriately, which could lead to a probe crash on the instrument.

FDAJan 19, 2009PR• Abbott Laboratories

Bosch and Siemens Dishwashers (BSH) – Fire Risk (2009)

This recall involves certain Bosch® and Siemens® dishwashers manufactured from May 1999 through July 2005. The brand name is printed on the dishwasher's front control panel. Model and serials numbers are located inside the dishwasher door panel on the upper right side. Brand Model Numbers Must Begin With Serial Numbers within the range of Bosch SHE43C, SHE44C SHE46C, SHE56C SHU33 SHU42 SHU432 SHU43C, SHU53A FD8503 - FD8507 FD8501 - FD8505 FD7905 - FD8505 FD8407 - FD8505 FD8004 - FD8211 FD8205 - FD8507 Siemens SL34A FD8308 - FD8505

CPSCJan 15, 2009Nationwide• BSH Home Appliances Corp., of Huntington Beach, Calif.

Stork Craft Baby Cribs (Stork Craft) – Entrapment Risk (2009)

This recall involves Stork Craft Baby cribs and Stork Craft cribs with the Fisher-Price logo. All Stork Craft Baby cribs with manufacturing and distribution dates between May 2000 and November 2008 are included in this recall. All Stork Craft cribs with the Fisher-Price logo have distribution dates between May 2000 and December 2004. The cribs were sold in various styles and finishes. The manufacture date, model number, crib name, country of origin, and the firm's name, address, and contact information are located on the assembly instruction sheet attached to the mattress support board. The firm's insignia "Storkcraft baby" or "storkling" is inscribed on the drop side teething rail of some cribs. In the product that contains the "Fisher-Price" logo, this logo can be found on the crib's teething rail, in the manufacturer's instructions, on the assembly instruction sheet attached to the mattress support board, and on the end panels of the Twinkle-Twinkle and Crystal crib models.

CPSCJan 13, 2009Nationwide• Stork Craft Manufacturing Inc., of British Columbia, Canada

Girls' Blue Denim Jackets (Ms. Bubbles) – Strangulation Risk (2009)

The recalled blue denim jackets have a white terrycloth underlay lining and drawstring. The jackets were sold in children's sizes medium (7-10), large (11-14) and x-large (15-16). Style numbers BF1400 K and BF1400 KP are printed on the hang tag attached to the garment.

CPSCJan 6, 2009Nationwide• Ms. Bubbles Inc., of Los Angeles, Calif.

BD Biosciences, Systems & Reagents: BD FACS Sample Prep Assistant (SPA and SPA II) Instrument...

To prevent a needle stick while replacing the probe, the firm has initiated a Field Correction, and issued an improved Users Guide procedure (User Bulletin, Part Number 645050).

FDAJan 3, 2009Nationwide• BD Biosciences, Systems & Reagents

Abbott Laboratories: Hematology Reagent Syringe, List number 08H49-02, used on...

Some syringes were improperly assembled and are therefore not usable, due to an incorrect nut on the syringe shell.

FDADec 10, 2008Nationwide• Abbott Laboratories

Bio-Rad Laboratories Inc: Bio-Rad Variant II Hemoglobin Testing System with CDM v 4...

The wrong barcode number and tube position number may be assigned to samples leading to discrepant sample results.

FDADec 9, 2008Nationwide• Bio-Rad Laboratories Inc

Bausch & Lomb Inc: Adapt AO, Akreos Advanced Optics Aspheric Lens. Bausch & ...

Affected lenses were inadvertently shipped to Bausch & Lomb's European Logistics Center (ELC) prior to release authorization. Initial testing indicated the product did not meet release criteria for endotoxin limits.

FDADec 8, 2008Nationwide• Bausch & Lomb Inc

Davol, Inc., Sub. C. R. Bard, Inc.: Bard 3D Max Mesh, Left large , Sterile Pre-formed Knitted...

Mislabeled: Product labeled as Left large, may contain a Right Large

FDADec 8, 2008Nationwide• Davol, Inc., Sub. C. R. Bard, Inc.

Abbott Laboratories: CELL-Dyn Ruby Hematology Analyzer, List Number 08H67-01 ...

Carryover failures in software revisions 1.0ML and 2.0ML result in elevated PLT background count.

FDANov 17, 2008Nationwide• Abbott Laboratories

Abbott Vascular-Cardiac Therapies dba Guidant Corporation: VOYAGER NC Coronary Dilatation Catheter, 4.5 X 8.0 mm. T...

The recall was initiated after Abbott Vascular received reports the protective, yellow balloon sheath of the 4.5mm diameter VOYAGER NC Coronary Dilatation Catheter has been tight. If unnoticed by the user, there is a potential to cause damage to the balloon dilatation catheter during removal of the sheath. The balloon sheath covers the balloon, maintaining the fold configuration and protects the

FDANov 5, 2008Nationwide• Abbott Vascular-Cardiac Therapies dba Guidant Corporation

Abbott Diabetes Care, Inc.: Abbott brand FreeStyle Navigator, Receiver Warranty Kit, ...

The product has the Units of Measure set to mmol/L rather than mg/dL. The blood glucose results could be misinterpreted. This may lead to under treatment and potential for hyperglycemia.

FDANov 1, 2008AZ, NY• Abbott Diabetes Care, Inc.

Duracell Notebook Power Adapters (Battery-Biz) – Burn Hazard (2008)

This recall involves the Duracell 130W Combo AC/DC adapters with model numbers EA10900, AC-6501, and DRUM130 and date codes 0804 and 0805. The black power adapter is used with notebook computers. "DURACELL UNIVERSAL POWER ADAPTER" is printed on the front of the power adapter. The model and date codes can be found on the rating label on the back of the power adapter.

CPSCOct 28, 2008Nationwide• Battery-Biz Inc., of Camarillo, Calif.

Abbott Laboratories, Inc: ACCELERATOR APS System Input/Output Module (IOM); List Nu...

When an ARCHITECT c16000 System is connected to an ACCELERATOR APS System, the software on the ACCELERATOR APS System may not generate an error warning when a Sample Presentation/Sample Queue error occurs, which could result in contamination of subsequent samples.

FDAOct 27, 2008Nationwide• Abbott Laboratories, Inc

Abbott Laboratories, Inc: ARCHITECT i1000SR" Processing Module System For In Vitro ...

During manufacturing, two components of the ARCHITECT i1000SR were reversed which could potentially cause falsely elevated patient results due to a sample-reagent and reagent-sample carryover.

FDAOct 21, 2008CO, FL, GA +11 more• Abbott Laboratories, Inc