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Ross Products Division, Abbott Laboratories

Ross Products Division, Abbott Laboratories Recalls

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

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Recall Summary

Total Recalls

1000

Past Year

567

Class I (Serious)

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 7501–7520 of 7756 recalls

Ross Products Division, Abbott Laboratories: Ross 22 FR Magna-Port Gastrostomy Tube, Item #51366.

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 18 FR Easy-Feed Gastrostomy Tube, Item #50114.

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 16 FR Easy-Feed Gastrostomy Tube, Item #50112.

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

FDA

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Nov 14, 2003

Nationwide

• Ross Products Division, Abbott Laboratories

Ross Products Division, Abbott Laboratories: Ross 18 FR Introducer Gastrostomy Kit with Brown Mueller ...

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 26 FR Gastrostomy Tube, Item #50158.

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 24 FR Gastrostomy Tube, Item #159.

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 28 FR Magna-Port Gastrostomy Tube, Item #54736.

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 18 FR Gastrostomy Tube, Item #154.

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 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, 2003Nationwide• 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

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

Baxa Corporation: Exacta-Mix 2400 pharmacy compounding system.

If device stops due to an alarm or operater pause, inlet valves will remain open, allowing some unwanted mixing of ingredients in the valve chamber..

FDANov 7, 2003Nationwide• Baxa Corporation

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

Beckman Coulter Inc: DataLink 2000 Data Manager

Software anomaly allows results to be archived prior to validation or to be uploaded to the lab information system.

FDANov 3, 2003Nationwide• Beckman Coulter Inc

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

Assay is imprecise.

FDANov 3, 2003Nationwide• Abbott Laboratories Diagnostic Div