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Davol, Inc., Sub. C. R. Bard, Inc.

Davol, Inc., Sub. C. R. Bard, Inc. Recalls

All product recalls associated with Davol, Inc., Sub. C. R. Bard, Inc..

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Recall Summary

Total Recalls

1000

Past Year

442

Class I (Serious)

138

Most Recent

Dec 2025

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 7121–7140 of 7663 recalls

Davol, Inc., Sub. C. R. Bard, Inc.: Davol Salute Reusable 18cm Shaft (Short/Open) Item Number...

Malformed constructs (straight shots) may form causing injury to user/patient

FDAJul 16, 2007Nationwide• Davol, Inc., Sub. C. R. Bard, Inc.

Davol, Inc., Sub. C. R. Bard, Inc.: Davol Salute Fixation Reusable Handle Item Code: 0113024...

Malformed constructs (straight shots) may form causing injury to user/patient

FDAJul 16, 2007Nationwide• Davol, Inc., Sub. C. R. Bard, Inc.

Davol, Inc., Sub. C. R. Bard, Inc.: Davol Salut Fixation Reusable 38cm Shaft (Laparoscopic) I...

Malformed constructs (straight shots) may form causing injury to user/patient

FDAJul 16, 2007Nationwide

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• Davol, Inc., Sub. C. R. Bard, Inc.

Davol, Inc., Sub. C. R. Bard, Inc.: Davol Salute Short 18cm Sterile Implant Cartridge - 10 Q-...

Malformed constructs (straight shots) may form causing injury to user/patient

FDAJul 16, 2007Nationwide• Davol, Inc., Sub. C. R. Bard, Inc.

Davol, Inc., Sub. C. R. Bard, Inc.: Davol Salute Laproscopic 38cm Sterile Implant Cartridge, ...

Malformed constructs (straight shots) may form causing injury to user/patient

FDAJul 16, 2007Nationwide• Davol, Inc., Sub. C. R. Bard, Inc.

Abbott Vascular-Cardiac Therapies dba Guidant Corporation: Multi-Link Vision RX Coronary Stent System, 3.0 x 15mm, P...

The affected single lot did not meet an internal specification. One unit failed the test criteria for stent dislodgment testing.

FDAJul 16, 2007Nationwide• Abbott Vascular-Cardiac Therapies dba Guidant Corporation

Power Tool Batteries (Milwaukee) – Laceration Risk (2007)

Laceration Risk

The recalled batteries are used to power drills, saws, radios, flashlights, wrenches and Extractor windshield glass removers. The recall includes 14.4- and 18-Volt 2.4Ah NiCd Milwaukee Power Plus, Chicago Pneumatic, and Extractor battery packs manufactured between July 1999 and February 2004. The brand name can be found on a label on most battery packs. However, some 14.4-Volt 2.4Ah packs did not have "Power Plus" on the label. The battery packs were sold both with tool kits and as individual battery packs. Battery packs manufactured after February 2004 are not included in this recall.

CPSCJul 11, 2007Nationwide• Milwaukee Electric Tool Co., of Brookfield, Wis.

Pacific Bioscience Lab, Inc.: Clarisonic Skin Care System - A hand held cleansing devic...

Overheating: The handle or charger/cradle can overheat, melting the plastic, which potentially can lead to smoke and fire and has caused mild user burns.

FDAJul 3, 2007IN• Pacific Bioscience Lab, Inc.

Thermador® Built-In Ovens (BSH Home Appliances) – Fire Risk (2007)

This recall involves Thermador® Brand built-in single ovens and combination models which have a conventional oven and a microwave. The model numbers of the single ovens are C271B, C301B, SEC271B and SEC301B. The model numbers of the combination models are SEM272B, SEM302B, SEMW272B and SEMW302B. The ovens have date codes between FD8403 and FD8701. The model number and date code can be found on the underside of the control panel.

CPSCJun 29, 2007Nationwide• BSH Home Appliances Corp., of Huntington Beach, Calif.

Ross Products Division Abbott Laboratories: The Companion ClearStar Pump System, for enteral feeding.

The transducer adapter bracket on the pump could crack or break and potentially result in under delivery of the enteral product.

FDAJun 21, 2007Nationwide• Ross Products Division Abbott Laboratories

Ross Products Division Abbott Laboratories: Embrace Enteral Pump

Continued use of the pump may cause the door pivot point on the back of the pump to crack or break. This will cause the pump to shut down and stop the initiation of enteral feeding.

FDAJun 21, 2007Nationwide• Ross Products Division Abbott Laboratories

Cardinal Health 303 Inc DBA Alaris Products: All IV Administration Infusion Sets intended for use with...

It has been determined that with low probability, over-infusion may occur as a result of an open safety clamp fitment (a.k.a. Flo-Stop fitment) on the pumping segment, whether opened intentionally in the course of expected clinical practice, or as a result of inadvertent action. The over-infusion occurrence is dependent on the user not closing the roller clamp first, as required by clinical practi

FDAJun 18, 2007PR• Cardinal Health 303 Inc DBA Alaris Products

Asko DW95 Model Series Dishwashers (Asko Cylinda) – Fire Risk (2007)

The recalled dishwashers include the ASKO model series DW95 with model numbers 1355, 1385, 1475, 1485, 1555, 1585, 1595, 1655, 1805, 1885, and 1895, manufactured from January 1995 through April 2000. The model number, serial numbers and manufacture date are printed on the name plate on the right interior side of the dishwasher door. Asko dishwashers manufactured after April 2000 are not included in the recall.

CPSCJun 14, 2007Nationwide• Asko Cylinda AB, of Vara, Sweden

Mountain Bicycles with Lefty Forks (Cannondale) – Fork Failure Risk (2007)

The carbon or aluminum bicycle forks were sold on Cannondale mountain bicycle models listed below: Bicycle model code, product Retail price Lefty Speed Carbon SL 2007 Taurine Carbon Team Replica 2007 Scalpel 1 2007 Scalpel Team Replica 2007 Rush Carbon 1 2007 Rush Carbon Team 2007 aftermarket, replacement Lefty Speed Carbon SL forks $5500 $5000 $5500 $6000 $6500 $1400 Lefty Speed DLR 2 (including bonded, 100mm and 80mm) 2007 Rush Carbon 2 (This model also included in the recall for Cranksets - CPSC press release #07-206) 2007 Rush 3 2007 Rush 4 2007 Rush 5 2007 Caffeine 29'er 2007 Scalpel 2 2007 Scalpel 3 2007 Caffeine 1 2007 Caffeine 2 2007 Rush Feminine 1 2007 aftermarket, replacement Lefty Speed (bonded, 100mm and 80mm) DLR 2 2008 Rush Carbon 3 $4500 $2600 $2100 $1700 $1600 $3500 $2600 $2200 $1600 $2000 $950 $3500

CPSCJun 13, 2007Nationwide• Cannondale Bicycle Corp., Bethel, Conn.

Bausch & Lomb Inc: Bausch & Lomb Zyoptix XP Epi Separator, packaged 1 per st...

Reports have been received of stromal incursions after use of the product.

FDAJun 8, 2007IN, MD, MN +2 more• Bausch & Lomb Inc

Bausch & Lomb Inc: Zyoptix XP Epi Head, packaged 1 per container, Cat. #ZXP3...

Reports have been received of stromal incursions after use of the product.

FDAJun 8, 2007IN, MD, MN +2 more• Bausch & Lomb Inc

Thermador Ceramic Cooktops – fire hazard (2007)

The cooktop has electric and induction heating elements with a black ceramic glass surface. This recall involves model numbers CIT302DS/01 and CIT362DS/01 with date codes between 8606 and 8612. The model number and date code can be found on the underside of the cooktop.

CPSCJun 7, 2007Nationwide• BSH Home Appliances Corp. of Huntington Beach, Calif.

Cardinal Health 303 Inc DBA Alaris Products: Alaris Medical Systems IV Administration Set, Low Sorbing...

The sterility of the product may be compromised as the packaging used for the sterility barrier was not designed for the sterility process used by the firm.

FDAJun 5, 2007Nationwide• Cardinal Health 303 Inc DBA Alaris Products

Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany: BrainLAB Target Positioner for Leksell Headring used with...

Target Alignment Error : A mechanical component/software incompatibility caused by a specific combination of the BrainLAB Target Positioner version 40700-3A for Leksell headrings and BrainLAB planning software resulted in a 1.25 mm shift in target area alignment during radiosurgery treatment.

FDAJun 5, 2007OH, WA• Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany

Boston Scientific Corporation One Boston: Boston Scientific Impulse Flextrusion Shaft 5F FR4 16391-...

Labels on the carton from two batches/lots of Impulse Angiographic Catheters may indicate a different curve style than the device that is actually in the carton.

FDAJun 4, 2007Nationwide• Boston Scientific Corporation One Boston