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Battery-Biz Inc., of Camarillo, Calif.

Battery-Biz Inc., of Camarillo, Calif. Recalls

All product recalls associated with Battery-Biz Inc., of Camarillo, Calif..

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Recall Summary

Total Recalls

1000

Past Year

276

Class I (Serious)

242

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 3621–3640 of 4099 recalls

Duracell Notebook Power Adapters (Battery-Biz) – Burn Hazard (2008)

Fire/Burn Risk

This recall involves the Duracell 130W Combo AC/DC adapters with model numbers EA10900, AC-6501, and DRUM130 and date codes 0804 and 0805. The black power adapter is used with notebook computers. "DURACELL UNIVERSAL POWER ADAPTER" is printed on the front of the power adapter. The model and date codes can be found on the rating label on the back of the power adapter.

CPSCOct 28, 2008Nationwide• Battery-Biz Inc., of Camarillo, Calif.

Intelerad Medical Systems Inc. 460 Ste-Catherine West Suite 210 Montreal Canada: IntelePACS Picture Archiving Communications System Intele...

Product software versions 3.5.2.P1 to 3.5.2.p56 inclusive and 3.6.1.P1 to 3.6.1.P82 inclusive were defective.

FDAOct 27, 2008Nationwide• Intelerad Medical Systems Inc. 460 Ste-Catherine West Suite 210 Montreal Canada

Murray Front Engine Riding Lawn Mowers (Briggs & Stratton) – Fire Hazard (2008)

1...180 181182183 184...205

Page 182 of 205Next

Fire/Burn Risk

This recall involves Murray front engine riding lawnmowers with the model and serial numbers listed below. The model and serial numbers are located on an identification tag on the rear frame of the unit. Model Serial Number Range 7800162 2012852329 through 2012852578; 2013004655 through 2013005154; 2013071338 through 2013071546 7800191 2012886982 through 2012887081; 2012887082 through 2012887231; 2013035588 through 2013035671 7800192 2012887399 through 2012887548; 2012887549 through 2012887648; 2012978024 through 2012978024; 2013046581 through 2013047179

CPSCOct 23, 2008Nationwide• Briggs & Stratton Power Products Group LLC, of Wauwatosa, Wis.

Advanced Sterilization Products: STERRAD 100S Sterilizer (Product Code 10101). The steril...

1) Inability of the sterilizer to detect when an injection takes place without hydrogen peroxide being transferred to the vaporizer bowl. This situation can result in a cycle completion with the injection of insufficient hydrogen peroxide sterilant and 2) Inability of the sterilizer to detect an obstruction in the door travel path while the door is closing. This situation can result in a hand b

FDAOct 17, 2008PR• Advanced Sterilization Products

Mindray DS USA, Inc., dba Datascope Patient Monitoring: AS3000 Anesthesia Delivery System. Datascope Patient Mon...

Two issues have been identified with the AS3000 unit. 1. The threadlocker of the caster (wheels) may not have been utilized, which may allow the caster to loosen and possibly separate from the unit. 2. The use of select brands of pre-pack absorber in the absorber canister of the AS3000 has been associated, in some cases, with gas leakage around the pre-pack, rather than through the absorber mate

FDAOct 7, 2008CA, IN• Mindray DS USA, Inc., dba Datascope Patient Monitoring

Advanced Sterilization Products: STERRAD NX Sterilizer, Product Code 10033 Low temperatur...

ASP has discovered a component defect in some of the UV lamp power supplies used in certain STERRAD NX Sterilizers. This defect can potentially cause the Hydrogen Peroxide Monitor to give inaccurate readings.

FDAOct 7, 2008AL, AZ, CA +14 more• Advanced Sterilization Products

Innovative Implant Technology: Sinu-Lift(TM) System, LLC., Model SLS-1, Sterile, Innovat...

Laceration Risk

Possible device failure: The cutter's shaft of the Sinu-Drill of the Sinu-Lift System could potentially get stuck inside the tap, thereby not allowing the cutter to spring out of the tap upon encountering the sinus membrane, increasing the possibility of perforating the sinus membrane.

FDASep 30, 2008Nationwide• Innovative Implant Technology

Medtronic Cardiovascular Revascularization & Surgical Therap: DLP(R) Pericardial/Intracardiac Sump Cannulae, 20 Fr., P/...

Separates: Six complaints were received from two locations. In all cases the sump tip assembly separated from the tubing during device removal and had to be retrieved from the patient. There were no adverse events affecting these patients.

FDASep 29, 2008IL, IN, IA +6 more• Medtronic Cardiovascular Revascularization & Surgical Therap

Ski-Doo Snowmobiles (BRP) – Drive Axle Failure (2008)

This recall involves Ski-Doo® Model Year 2008 and 2009 snowmobiles. Models included in the recall are listed below. Model numbers are printed on the side panels of the snowmobiles. Ski-Doo® Model Year 2008 MXZ X 800R PowerTEK MXZ X 600HO SDI MXZ Adrenaline 800R PowerTEK MXZ Adrenaline 600HO SDI MXZ TNT 500SS MXZ Trails 500SS GSX Limited Touring 600HO SDI GSX Limited 800R PowerTEK GSX Limited 600HO SDI GSX Sport 500SS MXZ Renegade X 800R PowerTEK MXZ Renegade X 600HO SDI MXZ Renegade 800R PowerTEK MXZ Renegade 600HO SDI Summit X 800R Power TEK Summit Everest 800R PowerTEK MXZ X 600RS Ski-Doo® Model Year 2009 MXZ TNT 600HO E-TEC

CPSCSep 26, 2008Nationwide• Bombardier Recreational Products Inc., of Valcourt, Canada

GE Healthcare Integrated IT Solutions: GE Healthcare Centricity Perinatal (formerly Quantitative...

Software anomalies in the Alert and Reminder feature could result in a delay of treatment. When attempting to select the last visible alert or reminder choice, the next choice on the list below the desired choice is selected, and an inconsistent color may be displayed for the same clinical element across a set of work stations.

FDASep 25, 2008Nationwide• GE Healthcare Integrated IT Solutions

GE Healthcare Integrated IT Solutions: GE Centricity PACS RA1000 Workstation (for diagnostic ima...

Software anomalies result in patient safety issues involving patient jacket content intermittently becoming unintentionally out of synchronization with the images being displayed, and involving Default Display Protocols (DDPs) which are used to layout images when displaying a study. If the user does not check the Study Date Time of the exam on the image title bar, then they may interpret the curr

FDASep 25, 2008Nationwide• GE Healthcare Integrated IT Solutions

GE Healthcare Integrated IT Solutions: Centricity Perinatal (formerly Quantitative Sentinel) Sys...

On the I&O chart, the IN, OUT and NET fluid totals values will not honor the numeric precision configuration, always displaying a whole number, losing decimal point accuracy.

FDASep 25, 2008Nationwide• GE Healthcare Integrated IT Solutions

Marine Elite Coolers (Igloo) – Laceration Risk (2008)

Laceration Risk

This recall involves Marine Elite coolers sold in white with stainless steel latches. The coolers were sold in four sizes: 72-quart, 94-quart, 128-quart and 162-quart.

CPSCSep 24, 2008Nationwide• Igloo Products Corp., of Katy, Texas

GE Healthcare Integrated IT Solutions: GE Centricity Ultra Laboratory System Software; for recor...

Software computer, error: The abnormal result flag is not being sent in the HL7 messages on results that are lower than the normal range. For further information, please telephone GE Healthcare Integrated IT Solutions at 800-437-1171.

FDASep 22, 2008Nationwide• GE Healthcare Integrated IT Solutions

Advanced Sterilization Products: ASP Automatic Endoscope Reprocessor, AER Plus Product Co...

Fire/Burn Risk

Residual high-level disinfectant solution remaining in endoscopes that have been reprocessed in the ASP Automatic Endoscope Reprocessor. If high-level disinfectant, or other fluids, remains in the endoscope after reprocessing, contact with the mucous membranes may occur and result in chemical burns, irritation (chemical colitis), or other symptoms.

FDASep 11, 2008PR• Advanced Sterilization Products

Cordless Screwdrivers (MasterForce) – fire burn risk (2008)

Fire/Burn Risk

The recalled cordless screwdrivers are green and gray in color. "MASTERFORCE" is printed on the top of the tool. "LITHIUM-ION TECHNOLOGY" and "241-0717" are printed on the handle.

CPSCSep 3, 2008Nationwide• Great Star Industry Co., of China

Wolf SL Carbon Bicycle Forks (True Temper) – Fall Hazard (2008)

The recalled forks have a clear coating over black painted carbon fiber, with the words "Wolf Superlite" and related logo just below the crown on each fork leg, and the letters "SL" on each leg above the fork blade dropouts. There is a True Temper CRT™ logo on the inside of both fork legs. The recalled forks could have been included on the following bicycle models: R3, R3 SL, Soloist Carbon, Soloist Carbon SL, and certain P3 Carbon framesets and complete bicycles.

CPSCAug 20, 2008Nationwide• True Temper Composite Material Products Co. Ltd, of Guangzhou, China

Innovative Neurotronics, Inc.: WalkAide Stimulator System Control Module, Part Number 20...

Knob responsible for regulating the amount of stimulation administered by the WalkAide System control unit may fall off while device is in use.

FDAAug 6, 2008Nationwide• Innovative Neurotronics, Inc.

Sunquest Information Systems, Inc.: Sunquest Laboratory System. Software Version: Sunquest ...

While performing in-house testing for the Sunquest Laboratory System and under certain conditions, there have been instances in which an error that occurred at the database level or originated in the operating system (Cache)was not communicated or displayed in the Graphic User Interface (GUI) application so the activity continued. While this error was registered in the error log in the System U

FDAAug 1, 2008Nationwide• Sunquest Information Systems, Inc.

Reebok Studio Exercise Cycles – Laceration Risk (2008)

Laceration Risk

The Reebok Studio Cycle is an upright exercise bike used primarily in fitness centers and other institutional settings. The recalled bicycle is black with silver cranks. The unit has an internal belt drive. The base of the bicycle is a single piece that is welded to the frame. The legs are two straight horizontal bars with rounded edges. There is a logo located on the side of the exercise cycle that shows a person riding a bicycle.

CPSCJul 24, 2008Nationwide• Fitness Associates Incorporated (F.A.I.), under license from Reebok International Ltd., of Canton, Mass. Note: F.A.I. is no longer in business.