Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Abbott Laboratories

Abbott Laboratories Recalls

All product recalls associated with Abbott Laboratories.

Get alerts for this brand

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 33841–33860 of 37665 recalls

Abbott Laboratories: Abbott CELL-DYN 3000 Hematology Analyzer

The product failed electrostatic discharge testing, which could result in product failure.

FDAMay 11, 2007PR• Abbott Laboratories

Halogen Table Lamps (Winsource) – Fire Hazard (2007)

Fire/Burn Risk

The recalled table lamps have a plastic base and two extendable arms connecting the base to a halogen lamp. The lamps were sold in white, red, blue, orange and purple. Item number 101988 is printed on the bottom of the lamp base.

CPSCMay 9, 2007Nationwide• Winsource Industries, Ltd., of Hong Kong

Stryker Howmedica Osteonics Corp.: ReUnion Fracture Stem Humeral Component - PureFix HA; Sho...

The plasma spray may delaminate from the proximal portion of the humeral stem.

FDA

1...1691 169216931694 1695...1884

Page 1693 of 1884Next

May 9, 2007

IN, OH

• Stryker Howmedica Osteonics Corp.

Heartfelt Carpet Tiles (InterfaceFLOR) – Puncture Hazard (2007)

The carpet tiles are made from a blend of wool and Kenaf, measure 20 inches by 20 inches and come in colors Corazon (beige), Herz (gray), and Coeur (light gray) The tiles have, "Made in USA" embossed on the bottom of each tile.

CPSCMay 9, 2007Nationwide• InterfaceFLOR LLC, LaGrange, Ga.

Datascope Corporation: The ClearGlide EVH small with Scissors. The kit includes ...

Datascope has experienced a higher than usual number of reports involving the Precision Bipolar Device. Reports include the locking or sticking of the buttons of the device which operate the jaws, particularly when a side load is placed on the shaft of the device.

FDAMay 7, 2007Nationwide• Datascope Corporation

Datascope Corporation: Precision Bipolar Device 6 pack Consists of a six-pack of...

FDAMay 7, 2007Nationwide• Datascope Corporation

Stryker Medical Div. of Stryker Corporation: Stryker Medical -Wheeled Electric Stretcher, Model 1550 (...

The internal power cord may become damaged due to wear and, if this occurs, a shock hazard exists.

FDAMay 7, 2007Nationwide• Stryker Medical Div. of Stryker Corporation

Datascope Corporation: Precision Bipolar Device ClearGlide EVH Small (endoscopic...

FDAMay 7, 2007Nationwide• Datascope Corporation

Beckman Coulter Inc: Cytomics FC 500 Flow Cytometry System with CXP Software V...

Incorrect Display: In certain modes, the protocol will not initially display the correct data in some plots. In addition, when running EWL files, any edited SampleID1 is not automatically updated in all tubes in the panel.

FDAMay 4, 2007Nationwide• Beckman Coulter Inc

Integra LifeSciences Corp.: Endura No-React Dural Substitute 2 cm x 10 cm

Integra LifeSciences Corporation d/b/a Integra NeuroSciences, the distributor of EnDura No-React Dural Substitute, manufactured by Shelhigh, Inc., Union, NJ, is recalling this product based on an FDA Public Health Notification and FDA requested recall letter to Shelhigh citing sterility and other manufacturing concerns regarding this product manufactured by Shelhigh. Integra is a distributor of t

FDAMay 4, 2007Nationwide• Integra LifeSciences Corp.

Intuitive Surgical, Inc.: Endoscopic Instrument Control System (da Vinci Surgical S...

Under certain circumstances, the product's software may crash and require a manual override or restart before functioning again. In addition, there is an unrelated addendum to the User Manual to clarify an icon not described in the previous User Manual.

FDAMay 3, 2007Nationwide• Intuitive Surgical, Inc.

Coast Spas (Coast Spas) – Fire Hazard (2007)

Fire/Burn Risk

The recalled spas were manufactured from January 2002 through October 2004. Only spas manufactured during this time frame with either red or yellow pump and motor assemblies are included in this recall. The spa manufacturer's name and date code and the pump and motor assembly can be located in the spa compartment as shown below. Consumers can access this compartment by lifting out the compartment door and setting it aside.

CPSCMay 3, 2007Nationwide• Coast Spas Manufacturing Inc., of Langley, British Columbia, Canada (spas)

Varian Medical Systems Inc: Varian Medical Systems Clinac Medical Linear Accelerator....

The wedge tray may slip out of the Clinac interface mount during gantry rotation.

FDAMay 2, 2007Nationwide• Varian Medical Systems Inc

Graco Baby Einstein Soft Blocks Tower – Choking Hazard (2007)

Choking Hazard

The soft block tower is a stack of three different shaped stuffed fabric blocks in red, yellow and blue. Pictures of apples, fire engines, ducks, bananas, birds and blueberries on the blocks are covered in plastic film. The soft blocks are one of nine toys that snap onto the tray of the activity center. Only model number 4635BEE with serial numbers 012705 through 063005, which indicates the manufacture dates of January 27, 2005 through June 30, 2005, are included in this recall. Model and serial numbers are located underneath the activity center's tray.

CPSCMay 2, 2007Nationwide• Graco Children's Products Inc., of Exton, Pa.

Airwalk Compel Clog Shoes (Payless) – Choking Risk (2007)

Choking Hazard

This recall involves Airwalk® Compel clog shoes sold in prewalk sizes 3 through toddler size 10. The flexible shoes have air ventilation holes on the top and side and plastic rivets with the Airwalk® logo attached to the strap. Airwalk® and the shoe size are printed on the sole of the shoe. No other sizes, styles or models are included in this recall.

CPSCMay 2, 2007Nationwide• Payless ShoeSource, Inc., of Topeka, Kan.

Ross Products Division Abbott Laboratories: Patrol enteral pump set with piercing pin, list #520540.

The enteral pump set may have a 1-3 mm slit in the silicone tubing located between the blue connector and the stretch band Safe-T-Valve.

FDAMay 2, 2007Nationwide• Ross Products Division Abbott Laboratories

Meretek Diagnostics, Inc.: BreathTek Urea Hydrolysis Rate Calculation CD, Version 1....

Diagnostic test kit for Helicobacter pylori was distributed for adult and pediatric use, but was not approved for pediatric use.

FDAMay 2, 2007Nationwide• Meretek Diagnostics, Inc.

Anima-Bamboo Collection Games (HaPe) – Lead Poisoning (2007)

This recall involves Anima-Bamboo Collection Games. The games contain 38 bamboo pads, four ghosts, and one dice. The product's packaging is an orange box with the words "Anima" and "BAMBOO Collection Games" printed on each side.

CPSCMay 2, 2007Nationwide• HaPe International Ltd., of Ningbo, China

Boston Scientific Corporation One Boston: Boston Scientific NexStent Monorail 5F Carotid Stent and...

Boston Scientific NexStent Carotid Stent device failed to deploy when the outer catheter (proximal outer and distal sheath) did not pull back and expose the self-expanding stent.

FDAMay 1, 2007Nationwide• Boston Scientific Corporation One Boston

Dental Equipment LLC: DCI Equipment Track Mount Light Assembly, 110v

Potential for light shield to melt due to light assemblies not properly rated to handle the VAC.

FDAMay 1, 2007IN, NY• Dental Equipment LLC