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Boston Scientific CRM Corp

Boston Scientific CRM Corp Recalls

All product recalls associated with Boston Scientific CRM Corp.

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Recall Summary

Total Recalls

1000

Past Year

893

Class I (Serious)

124

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 15101–15120 of 17593 recalls

Boston Scientific CRM Corp: Guidant Contak Renewal 3 CRT-D Model H170; 3CRT-D, Model ...

In April 2007, Boston Scientific CRM communicated with physicians regarding the potential for reduced Elective Replacement Indicator (ERI) to Battery End of Life (EOL) time in a subset of implantable defibrillators due to degradation of a low-voltage capacitor. Since that time, the April 2007 advisory population has not experienced any clinically significant changes to either the rate of occurrenc

FDAMar 4, 2009AL, AZ, AR +47 more• Boston Scientific CRM Corp

Trumpf Medical Systems, Inc.: ILED Surgical Light, Model numbers: ILED3, ILED5 and ILED5K

Cracks may form around the screw connections of the cover plates causing brittleness, which may lead to fragments breaking off and falling into the operating area.

FDAFeb 27, 2009Nationwide• Trumpf Medical Systems, Inc.

Concentric Medical Inc: Concentric 7F Balloon Guide Catheter (percutaneous cathet...

Product malfunction-- hub may leak at connection to the shaft due to insufficient adhesive curing.

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FDAFeb 27, 2009AL, FL, GA +11 more• Concentric Medical Inc

Scuba Diving Hoses (Ambient Pressure) – drowning risk (2009)

The crimped hoses are used to carry the air supply in the re-breathing diving system. The hoses were sold on three re-breathing models: Inspiration, Evolution and Evolution Plus. Hoses with a smooth (uncrimped) collar and with the model numbers listed below are included in the recall: AP300/15 ADV Supply Hose RB20/03 Oxygen Injection Hose EV20/03 Oxygen Injection Hose RB20/10 Buzzer Hose EV11A/1 Vision Handset Hose RB11A/1 Classic Handset Hose RB11/B Handset Hose AP300/10 ADV Hose AP300/38 ADV Hose Hoses with eight flats on the hose collar have been crimped and are not included in the recall.

CPSCFeb 24, 2009Nationwide• Ambient Pressure Diving Ltd., of Helston, Cornwall, United Kingdom

MDS Canada Inc. DBA MDS Nordion 447 March Road Ottawa Canada Ontario: TheraSphere Administration Set (Part Number K125914-034)....

Instructions for the use of the pinch clamp that is an integral part of the TheraSphere Administration Set were not included with the distribution of the device.

FDAFeb 24, 2009AZ, CA, CO +12 more• MDS Canada Inc. DBA MDS Nordion 447 March Road Ottawa Canada Ontario

Polymer Technology Systems, Inc.: PTS Panels CHOL+HDL Panel test strips for professional us...

Extended expiration date; the product expired on February 12, 2009 but was labeled with a April 4, 2009 expiration date.

FDAFeb 20, 2009Nationwide• Polymer Technology Systems, Inc.

Philips Medical Systems (Cleveland) Inc: TumorLoc software application, Software Versions: 23.1.1,...

A software anomaly in the TumorLoc software for the firm's Brilliance CT scanners was discovered. The same software anomaly was subsequently determined to be present in the firm's GEMINI PET/CT units. The software defect results in a the potential for data to be lost during reconstruction of images in which slices can either be discarded, or interleaved based upon their series ID.

FDAFeb 19, 2009Nationwide• Philips Medical Systems (Cleveland) Inc

Beckman Coulter Inc.: SYNCHRON Gentamicin (GEN) Reagent GEN reagent, when used ...

The reagent produces false low test results. Beckman Coulter has confirmed low recovery of values at the low end of the therapeutic range (<1.5 ug/mL, <3.13 umol/L) with SYNCHRON Systems Gentamicin Reagent (GEN) lot M804552. A false low result can cause a patient to receive more medication than necessary.

FDAFeb 19, 2009AL, AZ, AR +42 more• Beckman Coulter Inc.

Activity Centers (Evenflo) – fall hazard (2009)

The recall involves Evenflo ExerSaucer Triple Fun stationary activity centers made between October 2006 and December 2008. The model number is 6231711. Stage 3 position involves converting the product into an activity table. No other ExerSaucer models use end caps and, therefore, no other models are included in this recall.

CPSCFeb 17, 2009Nationwide• Evenflo Co. Inc., of Miamisburg, Ohio

Hooded Sweatshirts (Hill Sportswear) – strangulation risk (2009)

The recall includes the Kid Pullover Hood and Kid Zipper with Hood. The Kid Pullover Hood has a flat style drawstring at the neck, one middle front pocket, and fleece inside lining. Top sewn in label reads "HILL/ Made in USA." The hooded Zipper children's sweatshirt has a rounded style drawstring at the neck, two front pockets, and fleece inside lining. Top sewn in label reads "HILL/ Made in USA".

CPSCFeb 12, 2009Nationwide• Hill Sportswear Inc., of Paramount, Calif.

Diagnostic Chemicals, Ltd.: DCL (Diagnostic Chemicals Limited) Creatine Enzyme Reagen...

Labeled with extended expiration date (24 months instead of 18 months)

FDAFeb 12, 2009Nationwide• Diagnostic Chemicals, Ltd.

Cooking Systems (Jetboil) – burn hazard (2009)

Fire/Burn Risk

This recall involves personal and group cooking stoves often used during outdoor camping. The recalled models include: Personal Cooking Systems in black (PBL075-BLK-(PCS) and camo (PBL075-CAMO-(PCS), Backcountry Gourmet Set (BDLFRY), Personal Cooking System with Companion Cup (BDL001), Personal Cooking System with Pot Support & Stabilizer (BDL002), Personal Cooking System with Coffee Press (BDL003), and Personal Cooking System Java Kit (BDLJAVA) and Group Cooking System (GCS150).

CPSCFeb 11, 2009Nationwide• Jetboil Inc., of Manchester, N.H.

Halogen Clamp Lamps (Catalina Lighting) – Fire Hazard (2009)

Fire/Burn Risk

The halogen clamp lamps, also known as architect's lamps, have a 150-watt halogen bulb, an articulating arm, and a clamp desk lamp that adjusts up, down and swivels. Only lamps with model number 13456-US and lot numbers C06081581V185, C06081582V185 and C06081584V185 are included in the recall.

CPSCFeb 10, 2009Nationwide• Catalina Lighting Inc., of Miami, Fla.

Bicycle Forks (Marzocchi) – Crash Risk (2009)

The recalled bicycle forks were sold for installation on mountain bikes. The recall involves certain 2008 model year 888RC3 and 888RC3WC suspensions with date codes beginning with T07D07, T07D08 and T07D09. The forks are white or black with red and black artwork on the legs.

CPSCFeb 10, 2009Nationwide• Tenneco-Marzocchi s.r.l., of Bologna, Italy

Medtronic Sofamor Danek USA Inc: Medtronic INTREPID Spinal System SPACER, 32X23, 8 DEG, Si...

The firm received complaints regarding the use of the product in patients with poor bone quality, translational instability, difficulty implanting the cover plate and case of cover plate detachment.

FDAFeb 6, 2009Nationwide• Medtronic Sofamor Danek USA Inc

Computerized Medical Systems Inc: Focal Radiation Treatment Planning System, Focal Release...

Focal Software: if individual MLC leaf position edits are made, the original MLC aperture is retained. A subsequent aperture edit should not affect the MLC leaf positions however it was found that instead the leaves will then snap (unintentionally) back to the original aperture. Also, if the patient is sent to XiO after the MLC is edited, an isocenter shift made in XiO will also cause the MLCs to

FDAFeb 6, 2009Nationwide• Computerized Medical Systems Inc

Medtronic Sofamor Danek USA Inc: Medtronic SOFAMOR DANEK INTREPID SPINAL SYSTEM, 5.5MM TAP...

The firm received complaints regarding the use of the product in patients with poor bone quality, translational instability, difficulty implanting the cover plate and case of cover plate detachment.

FDAFeb 6, 2009Nationwide• Medtronic Sofamor Danek USA Inc

Digital Timers (Intermatic) – Shock Hazard (2009)

The recalled Intermatic DT17 heavy-duty digital timers are lamp and appliance timers. They were packaged as the "DT17C Heavy Duty Digital Timer" and the "DT17C8 Heavy Duty Digital Timer." The timer is white-colored and measures 3 3/8" tall x 2 5/8" wide x 1 5/8" deep. Only products with date codes of "40Z" through "52Z" or date codes ending in "A," "B" or "C" are included in the recall. The brand name "Intermatic" is molded on the front of the timer, and the model number ("DT17") and date code are printed on the back of the timer.

CPSCFeb 5, 2009Nationwide• Computime Ltd., of China

Cyberkinetics Neurotechnology Systems, Inc.: Cyberkinetics Inserter Wand & V2 Trigger Assembly, Expira...

Sterility of product cannot be assured

FDAFeb 4, 2009Nationwide• Cyberkinetics Neurotechnology Systems, Inc.

Medtronic Spine LLC, formerly Kyphon Inc: KyphX Xpander Inflatable Bone Tamp, size 15/3, Catalog Nu...

Product not sterile: 10 units were released for distribution without undergoing sterilization process.

FDAFeb 4, 2009FL, IN, OH• Medtronic Spine LLC, formerly Kyphon Inc