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
/
Ross Products Division, Abbott Laboratories

Ross Products Division, Abbott Laboratories Recalls

All product recalls associated with Ross Products Division, Abbott Laboratories.

Get alerts for this brand

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 4341–4360 of 4465 recalls

Ross Products Division, Abbott Laboratories: Ross 20 FR Magna-Port Gastrostomy Tube, Item #51364.

An increase in reported balloon failures, which may result in tube displacement.

FDANov 14, 2003Nationwide• Ross Products Division, Abbott Laboratories

Ross Products Division, Abbott Laboratories: Ross 14 FR Gastrostomy Tube, Item #152.

An increase in reported balloon failures, which may result in tube displacement.

FDANov 14, 2003Nationwide• Ross Products Division, Abbott Laboratories

Ross Products Division, Abbott Laboratories: Ross 20 FR Gastrostomy Tube, Item #155.

An increase in reported balloon failures, which may result in tube displacement.

FDANov 14, 2003

1...216 217218219 220...224

Page 218 of 224Next

Nationwide

• Ross Products Division, Abbott Laboratories

Ross Products Division, Abbott Laboratories: Ross 22 FR Easy-Feed Gastrostomy Tube, Item #50118.

An increase in reported balloon failures, which may result in tube displacement.

FDANov 14, 2003Nationwide• Ross Products Division, Abbott Laboratories

Abbott Laboratories HPD/ADD/GPRD: IMx Tacrolimus II Assay, list 3C10-20; Abbott Diagnostics...

Inadequate instructions for use resulting in calibration errors and the protein interference data in the package insert is not representative of assay performances.

FDANov 13, 2003Nationwide• Abbott Laboratories HPD/ADD/GPRD

Bausch & Lomb Inc: CX9625 Light Pipe (25 Gauge). The product is sold in pack...

The CX9625 Light Pipe connector may overheat; this condition could result in the plastic connector that plugs into the Millennium Microsurgical System to malfunction.

FDANov 10, 2003Nationwide• Bausch & Lomb Inc

Boehringer Laboratories Inc: Autovac TL. Autotransfusion System for Orthopedic Wound D...

Inadequate bond where the tube attaches to the inlet of the bulb.

FDANov 7, 2003CT, IL, IN +8 more• Boehringer Laboratories Inc

Bio Rad Laboratories, Inc.: Platelia Aspergillus EIA

Potential drug and device interaction with piperacillin/tazobactam (Zosyn) causing positive test result for galactomannan.

FDANov 6, 2003Nationwide• Bio Rad Laboratories, Inc.

Plan Toys Solid Drums (BRIO) – Design Problem (2003)

Choking Hazard

The recalled Plan Toys Solid Drum is natural wood with blue and red triangles painted on the side. The drum measures 6-1/4 inches in diameter and 3 inches high and has curved holes carved into the top. On the bottom of the drum are three rubber feet attached with screws. The recalled lot numbers are 46271068, 1546214 and 4345141 and are printed on the inside flap of the packaging. A stamp on the bottom of the drum displays the Plan Toys logo.

CPSCNov 6, 2003Nationwide• BRIO® Corp., of Germantown, Wis., a subsidiary of BRIO AB of Sweden

Abbott Laboratories HPD/ADD/GPRD: Architect Anti-HBs Reagent Kit; list 7C18-25, 100 tests a...

Aspiration errors in the conjugate component due to microbial contamination of the conjugate.

FDANov 5, 2003Nationwide• Abbott Laboratories HPD/ADD/GPRD

Abbott Laboratories Diagnostic Div: AEROSET Phenobarbital, LN 1E08-01

Assay is imprecise.

FDANov 3, 2003Nationwide• Abbott Laboratories Diagnostic Div

Abbott Laboratories, Inc: The AXSYM System, Clinical Chemistry Analyzer, Manufactur...

Potential for a contaminated Reaction Vessel (RV) or previously used RV to remain on the AxSYM System.

FDAOct 29, 2003Nationwide• Abbott Laboratories, Inc

Abbott Laboratories, Inc: AEROSET System Software version 1.02ER000

Audible alarm occurs before aspiration potentially resulting in operator injury or results assigned to wrong patient for STAT samples.

FDASep 30, 2003Nationwide• Abbott Laboratories, Inc

Abbott Laboratories HPD/ADD/GPRD: IMx Tacrolimus II Calibrators, list 3C10-10; the pack con...

Invalid test results are being generated due to calibration errors when using calibrator lots 94165M100 and 94164M100.

FDASep 19, 2003Nationwide• Abbott Laboratories HPD/ADD/GPRD

Toy Necklaces (L.M. Becker) – Pendant Hazard (2003)

The necklaces consist of a 10-inch black cord with a 7/8- inch-diameter gray metal pendant. The metal pendant has assorted symbols on one side.

CPSCSep 10, 2003Nationwide• L.M. Becker and Co. Inc., of Kimberly, Wis.

Bausch & Lomb Incorporated: Phaco Needles, catalog #DP8115, with 15 degree needle ta...

The firm's DP8200 Microflow Needle Packs were labeled with the firm's DP8115 Phaco Needle Packs and visa versa.

FDAAug 25, 2003FL, IL, IN +3 more• Bausch & Lomb Incorporated

Bausch & Lomb Incorporated: Microflow Needles, catalog #DP8200, with 0 degree taperin...

The firm's DP8200 Microflow Needle Packs were labeled with the firm's DP8115 Phaco Needle Packs and visa versa.

FDAAug 25, 2003FL, IL, IN +3 more• Bausch & Lomb Incorporated

Abbott Laboratories HPD/ADD/GPRD: AxSYM Homocysteine Reagent Pack, list 5F51-20, Produced b...

There is a kit-to-kit difference within the lots, with the reagents generating different polarization values than those in others.

FDAAug 22, 2003Nationwide• Abbott Laboratories HPD/ADD/GPRD

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

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.

FDAJul 21, 2003Nationwide• Abbott Vascular Devices