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Boston Scientific Corporation

Boston Scientific Corporation Recalls

All product recalls associated with Boston Scientific Corporation.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

145

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 36321–36340 of 37661 recalls

Boston Scientific Corporation: Titanium Dual Lumen Implantable Port with PASV Valve and ...

Catheters may not have adequate radiopacity for proper visualization under fluoroscopy.

FDAMar 29, 2004Nationwide• Boston Scientific Corporation

Deltec, Inc: ProPort Low Profile Plastic Venous Access System, with Po...

Some of the outer product pouches have voids in the seals and do not assure that the outer surfaces of the inner tray containing the port, catheter and procedural components remain sterile after sterilization.

FDAMar 29, 2004Nationwide• Deltec, Inc

Deltec, Inc: Port-A-Cath Low Profile Titanium Venous Access System, w...

1...1815 181618171818 1819...1884

Page 1817 of 1884Next

FDA

Mar 29, 2004

Nationwide

• Deltec, Inc

HID Light Fixtures (Lithonia) – Installation Risk (2004)

These are Indoor HID light fixtures with acrylic lenses and/or reflectors. They are generally used in industrial and commercial locations such as retail spaces, warehouses, and gymnasiums. Only certain models of specific wattage lights are included in the recall. Check the Lithonia website for a list of the specific model and wattage combinations included. All recalled fixtures were manufactured in Crawfordsville, Indiana, and have a date of manufacture from November 2002 through October 2003. The models, wattages, city and date of manufacture, and "Lithonia" can be found on a label attached to the ballast housing. This recall also includes certain ballast repair kits.

CPSCMar 29, 2004Nationwide• Lithonia Lighting, of Conyers, Ga.

Deltec, Inc: Port-A-Cath Titanium Venous Access System, with Silicone...

FDAMar 29, 2004Nationwide• Deltec, Inc

Deltec, Inc: Port-A-Cath P.A.S. Port T2 Titanium Venous Access System,...

FDAMar 29, 2004Nationwide• Deltec, Inc

Abbott Laboratories HPD/ADD/GPRD: AxSYM Troponin-I Reagent Kit, list 3C29-20, 100 test kit;...

Laceration Risk

An increase in complaints of higher than normal patient results, some from the healthy population range to above the diagnostic cutoff for an Acute Myocardial Infarction.

FDAMar 26, 2004Nationwide• Abbott Laboratories HPD/ADD/GPRD

Medtronic Perfusion Systems: Medtronic Trillium Affinity NT Integrated-CVR Membrance O...

An incorrect date of manufacture and incorrect use-by date were printed on the labels of the pouches used for the product.

FDAMar 25, 2004Nationwide• Medtronic Perfusion Systems

Window Air Conditioners (Fedders) – Electrical Issue (2004)

Fire/Burn Risk

The units included in the recall are 8,000 BTU window air conditioners with electric heat, sold under the brand names and model numbers shown below. The model and serial number is located on the air conditioner cabinet near the bar code. The serial number of included units of the listed models begin with the following two letter code: Brand Name Model Number Serial Number Begins With Fedders AEQ08F2E AR, AS, ER, HR, JP, KP Maytag MEQ08F2E AR, AS, ER, FR, KR, KP, LR, MP, MR Comfort-Aire RED-81 DR, ER, KP, KR, LP

CPSCMar 25, 2004Nationwide• Fedders Corporation, of Liberty Corner, N.J.