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Boston Scientific Corp

Boston Scientific Corp Recalls

All product recalls associated with Boston Scientific Corp.

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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 32281–32300 of 37665 recalls

Boston Scientific Corp: Boston Scientific Stonetome Stone Removal Device. Triple...

The ultraviolet light barrier on the pouch may be discolored, which will allow ultraviolet light into the package and may cause the latex retrieval balloon to become brittle and to leak or burst when inflated.

FDAJan 8, 2009Nationwide• Boston Scientific Corp

Stryker Howmedica Osteonics Corp.: Super Secur Fit Plus. Hip stems are single use devices i...

Product deviation : Specific lots of sprayed HA hip stems did not meet Stryker's Internal Material Specification for tensile bond strength and crystallinity.

FDAJan 6, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Accolade TMZF Hip Stem; Hydroxylapatite Coated, Titanium ...

Product deviation : Specific lots of sprayed HA hip stems did not meet Stryker's Internal Material Specification for tensile bond strength and crystallinity.

1...1613 161416151616 1617...1884

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FDAJan 6, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Accolade TMZF Plus Hip Stem; Hydroxylapatite coated, Tita...

Product deviation : Specific lots of sprayed HA hip stems did not meet Stryker's Internal Material Specification for tensile bond strength and crystallinity.

FDAJan 6, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Citation TMZF HA Hip Stem - LT. Hip stems are single use...

Product deviation : Specific lots of sprayed HA hip stems did not meet Stryker's Internal Material Specification for tensile bond strength and crystallinity.

FDAJan 6, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Omniflex-HA Hip Stem W/C Taper. Hip stems are single use...

Product deviation : Specific lots of sprayed HA hip stems did not meet Stryker's Internal Material Specification for tensile bond strength and crystallinity.

FDAJan 6, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Citation TMZF HA Hip Stem - RT. Hip stems are single use...

Product deviation : Specific lots of sprayed HA hip stems did not meet Stryker's Internal Material Specification for tensile bond strength and crystallinity.

FDAJan 6, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Jardine Cribs (Jardine) – Entrapment Risk (2009)

This recall involves three models of Jardine wooden cribs with the date codes identified below. Cribs with other date codes are not affected by this recall. The date code and model number are printed on the label located on the inside of the bottom rail of the headboard or footboard. Jardine Cribs included in this Expanded Recall Model # Description Date Code Between DA715BC Dark Pine Olympia Lifetime Crib 2/04 - 1/07 0108L00 Antique Walnut Capri Single Crib 7/06 - 11/07 0308C00 White Capri Lifetime Crib 12/05 - 11/07

CPSCJan 6, 2009Nationwide• Jardine Enterprises, of Taipei, Taiwan

Stryker Howmedica Osteonics Corp.: Short Citation TMZF HA Hip Stem - Right; Hydroxylapatite ...

Product deviation : Specific lots of sprayed HA hip stems did not meet Stryker's Internal Material Specification for tensile bond strength and crystallinity.

FDAJan 6, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Medical Div. of Stryker Corporation: Stryker InTouch 1.0 Zoom Critical Care Bed; Model 2140. ...

The touch screen on the footboard may display a "tilt over range" error, resulting in a precautionary stop of the bed motions which result in the bed appearing to have locked out some of its bed positioning features.

FDAJan 5, 2009Nationwide• Stryker Medical Div. of Stryker Corporation

Stryker Medical Div. of Stryker Corporation: Stryker InTouch 1.0 Critical Care Bed; Model 2130. The d...

The touch screen on the footboard may display a "tilt over range" error, resulting in a precautionary stop of the bed motions which result in the bed appearing to have locked out some of its bed positioning features.

FDAJan 5, 2009Nationwide• Stryker Medical Div. of Stryker Corporation

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

Wiring Books (Taunton Press) – Electrical Shock Risk (2008)

The recall involves the 3rd Edition of Wiring a House. The paperback book's cover is white and yellow and has a photograph of a man wiring a panel. ISBN #978-1-56158-942-5 is printed on the back cover. Wiring Complete, Expert Advice from Start to Finish is paperback and has a green, black and white cover that shows hands wiring an electrical wall receptacle. "Taunton's" is printed at the top. ISBN #978-1-56158-815-2 is printed on the back cover.

CPSCDec 30, 2008Nationwide• The Taunton Press, of Newtown, Conn.

Philips Medical Systems North America Co. Phillips: Philips Medical Systems MultiDiagnost Eleva Flat Detector...

System fails to meet requirements when it is used at kV levels greater than 115 kV at certain frame rates and in certain acquisition modes, as grid switch leakage may occur.

FDADec 30, 2008Nationwide• Philips Medical Systems North America Co. Phillips

Fire Alarm Control Panels (Notifier) – Alert Failure (2008)

This recall involves the Notifier brand operating system firmware control panels in fire alarms. The control panel is black or red with a silver screen. The panels control display and emergency communications. "NOTIFIER" or "NOTIFIER by Honeywell" is printed on the front of the fire alarm unit. This recall includes the following model numbers: Firmware version 11.2.2 for NFS2-640 and NFS-320 control panels and firmware version 3.14.1 for and NFS-640 control panels.

CPSCDec 30, 2008Nationwide• Notifier, of Northford, Conn.

Boston Scientific Corp: Boston Scientific EndoVive 20F (6.7 mm) Safety PEG Kit, P...

The user may be unable to pass the device over the guidewire for placement in the patient, resulting in an inability to use the device.

FDADec 30, 2008Nationwide• Boston Scientific Corp

Boston Scientific Corp: Boston Scientific EndoVive 24F (8 mm) Safety PEG Kit, Pus...

The user may be unable to pass the device over the guidewire for placement in the patient, resulting in an inability to use the device.

FDADec 30, 2008Nationwide• Boston Scientific Corp

Quality Electrodynamics Llc: Mirror assembly to magnetic resonance device (1.5T Atlas ...

The firm received a complaint indicating that the mirror is high risk and could drop on a patient.

FDADec 29, 2008Nationwide• Quality Electrodynamics Llc

Philips Healthcare Informatics, Inc.: iSite PACS (Picture Archiving and Communications System) ...

Product may display clinical reports with the study date and time in GMT format, which may not be obvious to the end user, who may expect to see the local time in the report.

FDADec 29, 2008Nationwide• Philips Healthcare Informatics, Inc.

Stryker Endoscopy: Pnemosure Insufflators, model numbers 620-040-600 and 620...

Unexpected powering down/failure to boot up: A problem with a transistor in the heater/temperature sensor component in the device may cause the device to power off during surgery or to fail to boot up at all. The risk includes delay and interruption of ongoing surgical procedures.

FDADec 29, 2008Nationwide• Stryker Endoscopy