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DEWALT Industrial Tool Co., of Towson, Md.

DEWALT Industrial Tool Co., of Towson, Md. Recalls

All product recalls associated with DEWALT Industrial Tool Co., of Towson, Md..

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

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 23321–23340 of 25000 recalls

Portable Generators (DEWALT) – Electric Shock Risk (2007)

The recall involves DEWALT DG2900 2900-watt gasoline-powered generators with date codes 200150 through 200635. The generators are black and yellow. "DEWALT" and "DG2900" are printed on the generator. The date code is stamped on the right side of the unit on the black plastic covering the rear of the control panel. Units with an "R" stamped on the name plate are not affected by this recall.

CPSCJan 4, 2007Nationwide• DEWALT Industrial Tool Co., of Towson, Md.

Abbott Laboratories MPG: ARCHITECT i System Assay CD-ROM, in vitro diagnostic anal...

The ARCHITECT AUSAB and ARCHITECT Anti-HCV assay parameter default interpretation screens when using ARCHITECT Assay CD-ROM US Version 06E58-21 does not align with the result interpretation options in the ARCHITECT AUSAB Reagent Package Insert (PI) 34-4162/R1 and ARCHITECT Anti-HCV PI 34-4152/R1.

FDAJan 2, 2007Nationwide• Abbott Laboratories MPG

Becton Dickinson and Company: BD Beaver Mini-Blade, Blade Sharp Two Sides Pointed, Cat...

1...1165 116611671168 1169...1250

Page 1167 of 1250Next

Product sterility may be compromised due to incomplete package seal

FDADec 26, 2006Nationwide• Becton Dickinson and Company

Becton Dickinson and Company: BD Beaver Mini-Blade, Mini/Bulk 64, Catalog Number: 374820

Product sterility may be compromised due to incomplete package seal

FDADec 26, 2006Nationwide• Becton Dickinson and Company

Becton Dickinson and Company: BD Beaver Mini-Blade, Blade Mini Orthopedic 1.255 in, Cat...

Product sterility may be compromised due to incomplete package seal

FDADec 26, 2006Nationwide• Becton Dickinson and Company

Abbott Molecular: Vysis LSI ATM/p53: D13S319 /CEP 12/13q34 DNA Probe Set; f...

The LSI D13S319 SO/13q34 SA/CEP 12 SG probe of the two mixture DNA-Probe was contaminated with LSI ATM SG/p53 SO probe. This contamination would result in 10 FISH signals in each normal cell rather than the expected 6 FISH signals in each normal cell.

FDADec 22, 2006Nationwide• Abbott Molecular

Advanced Neuromodulation Systems, Inc: Eon Rechargeable Implantable Pulse Generator (IPG) System

Product's external charging system on occasion was failing to communicate with the Implantable Pulse Generator preventing re-charging of the pain relief system.

FDADec 22, 2006Nationwide• Advanced Neuromodulation Systems, Inc

GE Medical Systems LLC: Definium AMX 700 Digital mobile x-ray system, GE Healthca...

When using the Tech Switch on exposures >750ms, >100 kVp and > 100 mAs the exposure terminates prematurely.

FDADec 21, 2006IN, MS, NE +2 more• GE Medical Systems LLC

Reciprocating Saws (DEWALT) – Fire Hazard (2006)

Fire/Burn Risk

This recall involves cordless DEWALT DC305 model reciprocating saws with date codes 200601-49 through 200640-49. They are yellow and black and about 18 inches long. The model number is located on the name plate on the side of the housing and the date code is located under the handle where the battery is inserted.

CPSCDec 21, 2006Nationwide• DEWALT Industrial Tool Co., of Towson, Md.

Cut-Out Tools (DEWALT) – Shock Hazard (2006)

Laceration Risk

These DEWALT cut-out tools are yellow and black, and have model number DW660 written on their nameplate, which is located on the body of the unit. The recalled tools were manufactured between January 2006 and September 2006, and have date codes ranging from 200601 to 200639. The date code also is located on the tool's nameplate. Units with a "V" stamped on the nameplate are not included in this recall.

CPSCDec 21, 2006Nationwide• DEWALT Industrial Tool Co., of Towson, Md.

Integrated Orbital Implants Inc: Perry-Kolberg Titanium Motility/Support System (Threaded ...

The threads on the threaded sleeve were manufactured with left-handed threads, requiring a modification to the surgical technique for proper insertion. Failure to properly identify the affected components and apply the modified insertion technique will result in an inability to insert the sleeve into the implant.

FDADec 20, 2006Nationwide• Integrated Orbital Implants Inc

Toshiba American Med Sys Inc: Nemio XG, ultrasound system, SSA-590A with version 1.5 so...

Transducer Surface Temperature : It was found during testing that when using the system in the 2DCDI + PW mode, with the Scale Graph function active, that the transducer surface temperature could exceed the 27 degrees Celsius limit as specified in the IEC safety standard.

FDADec 19, 2006Nationwide• Toshiba American Med Sys Inc

Philips Medical Systems: HeartStart FR2+ Defibrillator

Potential for shock treatment to be delayed or prevented due to board contamination that causes intermittent switch operation

FDADec 19, 2006Nationwide• Philips Medical Systems

Medtronic Sofamor Danek Instrument Manufacturing: Rocker Reducer, part of the SiLo Spinal System, REF 88800...

Due to a manufacturing error, the proximal end may deform causing the protrusions that engage the associated implant to break off of the instrument during use.

FDADec 18, 2006Nationwide• Medtronic Sofamor Danek Instrument Manufacturing

Terang Nusa Sdn Bhd 1, Jalan 8, Pengkalan Chepa 2, Ind Zone Kota Bharu Malaysia: Sterile Neolon 2G Latex-Free Powder-Free Neoprene Surgica...

Some of the packages labeled as latex-free actually contain latex gloves.

FDADec 18, 2006Nationwide• Terang Nusa Sdn Bhd 1, Jalan 8, Pengkalan Chepa 2, Ind Zone Kota Bharu Malaysia

Suros Surgical Systems Inc.: Suros ATEC Breast Biopsy System handpiece (9 gauge cannul...

The handpiece package may have an incorrect part number on the inner package. Error could result in over-penetration of the biopsy needle.

FDADec 15, 2006Nationwide• Suros Surgical Systems Inc.

Pressure Washers (DeVilbiss) – Fracture Risk (2006)

Laceration Risk

The recalled pressure washers and air compressors were sold under the following brands and model numbers: Brand Model Numbers Manufacture Dates Pressure washers Delta DTH2450, DTH2450-1, D2750H, D2400H-2, D2400H-3, D2700K-1, DTT2450 1/27/04 through 8/3/05 Excell XR2750-1, XR2600, XR2600-1, XR2600-2, XR2500-1 1/26/04 through 11/2/05 Porter-Cable PCV2250-2, PC2525SP-1, PCE1700-3, PCH2401-1, PCK3030SP-1, PCV2500, PCH2800C, PCE1700-2, PCH2425-2 6/4/04 through 10/24/05 Pressure-Wave PWH2500, PWH2500K 1/6/05 through 10/31/05 Water Driver WHAB2627-1 6/11/04-7/19/05 Air Compressors Porter-Cable CFFR350B-1, C3151-1, C3551-1, PTA51 Service Kit December 16, 2004 to May 5, 2006 On the pressure washers, the brand, model number and manufacturing date are located on the name plate on the rear of the engine base and on the air compressors they are located on the front of the motor housing. Only pressure washers and compressors with pneumatic tires with plastic tire hubs are affected; pressure washers and compressors with solid tires or metal tire hubs are not affected.

CPSCDec 15, 2006Nationwide• DeVilbiss Air Power Company, of Jackson, Tenn.

Bausch & Lomb Inc: Bausch & Lomb Millennium 20 Ga. High Speed Posterior Vitr...

Laceration Risk

The cutter tip could break during a procedure

FDADec 14, 2006Nationwide• Bausch & Lomb Inc

Philips Medical Systems North America Co. Phillips: Allura Mono X-Ray System, angiographic - monoplane, analo...

Movement of the AD5 table or Lateral C-arm (LARC). The table and/or LARC will not move upon request, will move slowly when movement is requested or will not stop moving when requested.

FDADec 14, 2006Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: FD 20/10 X-Ray System, Angiograph, biplane, digital Allur...

Movement of the AD5 table or Lateral C-arm (LARC). The table and/or LARC will not move upon request, will move slowly when movement is requested or will not stop moving when requested.

FDADec 14, 2006Nationwide• Philips Medical Systems North America Co. Phillips