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Dade Behring Inc. Rte 896, Glasgow Business Community

Dade Behring Inc. Rte 896, Glasgow Business Community Recalls

All product recalls associated with Dade Behring Inc. Rte 896, Glasgow Business Community.

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Recall Summary

Total Recalls

1000

Past Year

898

Class I (Serious)

125

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 16821–16840 of 17592 recalls

Dade Behring Inc. Rte 896, Glasgow Business Community: StreamLab Analytical Workcell. General Purpose Laboratory...

Software can sample the incorrect specimen from the StreamLAB to the Dimension RxL or RxL Max Systems.

FDANov 12, 2004IL, IN, MD +3 more• Dade Behring Inc. Rte 896, Glasgow Business Community

B & K Medical Systems Inc.: Linear Array Transducer Type: 8809

Defect at probe tip may effect sterilization and electrical safety

FDANov 12, 2004CA, CO, CT +7 more• B & K Medical Systems Inc.

Proctor & Gamble Co: The product is battery powered toothbrush. Spinbrush Pro ...

Market withdrawal of Crest Spinbrush Pro-Whitening. The firm has determined that there is a quality issue in certain production that may allow the circular brush at the tip of the brush head to become detached over time in a very small number of brushes.

FDA

1...840 841842843 844...880

Page 842 of 880Next

Nov 11, 2004

Nationwide

• Proctor & Gamble Co

Smiths Medical MD, Inc.: Deltec branded PORT-A-CATH II Single-Lumen Low Profile Po...

The catheter became disconnected from the port while implanted in the patient.

FDANov 11, 2004FL, GA, IN +8 more• Smiths Medical MD, Inc.

The Straumann Company: Straumann Dental Implant System, SP Profile Drill, Short,...

Outside label incorrectly identifes drill as Regular Neck (RN) instead of Wide Neck (WN)

FDANov 11, 2004Nationwide• The Straumann Company

Proctor & Gamble Co: The product is refill heads for battery powered toothbrus...

FDANov 11, 2004Nationwide• Proctor & Gamble Co

Alaris Medical Systems Inc: Model 8100 Series Medley Medication Safety System Pump Mo...

The device modification is being implemented in response to information received from the field regarding a specific method of misloading the medication administration tubing set into the infusion system pump module. To date there have been complaints from three (3) different customer locations.

FDANov 10, 2004Nationwide• Alaris Medical Systems Inc

Vermont Castings Barbeque Grill – Potential Failure (2004)

Fire/Burn Risk

The recalled grills have five burners and a label on the back of the cabinet, with the model number on the left side. Models CF9086 and VCS5000 are equipped with a side burner. Model CF9085 is not equipped with a side burner. Grills that do not have five burners and grills sold before 2004 are not affected by this recall. All of the affected grills were listed by Canadian Standards Association.

CPSCNov 10, 2004Nationwide• CFM Corporation, of Mississauga, Ontario, Canada

Precision Medical, Inc.: Easy Go Vac Aspirator, Model PM65. Portable suction unit

Battery charger can be overcharged and overheat

FDANov 9, 2004Nationwide• Precision Medical, Inc.

Soliras Headlamp Batteries (Black Diamond) – Battery Issue (2004)

Fire/Burn Risk

The recalled batteries are found in Black Diamond Soliras headlamps. The batteries have the following dates, which can be found on the battery label: 0703, 0803, 0903, 1003, 1103, 1203, 0104, 0204, 0304, 0404, and 0504. The black headlamp has the words and symbol for the company on the light.

CPSCNov 9, 2004Nationwide• Black Diamond Equipment Ltd., of Salt Lake City, Utah

John Deere Gator HPX Utility Vehicle – Safety Defect (2004)

Gator HPX Utility Vehicles are four wheeled vehicles with a cargo box. The words "John Deere", "Gator" and "HPX" appear on the cargo box. The following model and serial numbers can be found on the serial number plate on the vehicle's frame: Model Serial Range HPX 4X2 Gas M0HP2GX010001-010775 HPX 4X2 Diesel M0HP2DX010001-030032 HPX 4X4 Gas M0HP4GX010001-031406 HPX 4X4 Diesel M0HP4DX010001-030552 HPX 4X4 Trial M0HP4GT010001-030678

CPSCNov 9, 2004Nationwide• Deere & Company, of Moline, Ill.

Beckman Coulter Inc: Access Immunoassay Systems, 862.2160 discrete photometric...

A rare condition of the Access 2 Immunoassay Systems software versions 2.0, 2.1 and 2.2 could present a risk of an erroneous confirmatory result under a specific set of circumstances. The Chlamydia Blocking results may be affected. The instrument will erroneously perform the blocking calculation on the affected test by using the mean of the diluted and neat results.

FDANov 8, 2004Nationwide• Beckman Coulter Inc

Beckman Coulter Inc: DL2000 Data Manager Software, Version 6.4.108

Possibility of reporting an incorrect result occurs due to a software anomally.

FDANov 5, 2004CA, FL, IL +1 more• Beckman Coulter Inc

Brake Parts Cleaner (Valvoline) – Chemical Risk (2004)

The recall involves 13-ounce cans of Pyroil® Non-Chlorinated Brake Parts Cleaner and NAPA® Non-Chlorinated Brake Cleaner. This product is used by professional mechanics as well as "do-it-yourself" consumers who perform brake repairs on their own vehicles. The recalled cans contain one of the following four digits in their date codes, which are found on the bottom of the cans: Pyroil (Part No. 4003) C014 C024 C184 C194 C304 D024 D034 D214 D224 D264 E104 F074 F084 F094 F104 F234 F244 F284 G134 G144 G194 G294 H034 H194 NAPA (Part No. 4800) C024 C094 C184 C194 C224 C234 C304 C314 D014 D034 D054 E054 E064 E144 E244 E254 F174 F184 G284 H124 H304 H314 I074 I084

CPSCNov 4, 2004Nationwide• The Valvoline Company, a Division of Ashland Inc., of Lexington, Ky.

Hampton Bay Halogen Light Fixture – Safety Issue (2004)

Fire/Burn Risk

The recall involves the Hampton Bay® three-head, flush-mount, halogen light fixture with silver metal rings on the lamp fixtures. It is 15.75 inches wide by 6 inches high. The lights have frosted glass shades. The position of the three lamps on the fixture can be adjusted by turning and bending the lamp heads. A clear label on the fixture reads "MADE IN CHINA," and "E91785."

CPSCNov 4, 2004Nationwide• Cordelia Lighting, of Rancho Dominguez, Calif.

Bard Access Systems, Inc: Site-Rite Sterile Ultrasound Probe Cover with Gel

Conductivity gel pouches, labeled as sterile, and packaged in various needle guide kits may not be sterile.

FDANov 3, 2004Nationwide• Bard Access Systems, Inc

Bard Access Systems, Inc: Site Rite II, Site Rite 3, and Site Rite IV Systems with ...

Conductivity gel pouches, labeled as sterile, may not be sterile.

FDANov 3, 2004Nationwide• Bard Access Systems, Inc

Bard Access Systems, Inc: Ultra/Phonic Conductivity Gel, 20 ml. Each unit is a foi...

Conductivity gel pouches, labeled as sterile, may not be sterile.

FDANov 3, 2004Nationwide• Bard Access Systems, Inc

Access CardioSystems: AccessAED PAD (without ECG trace) -Public Access Defibril...

Device may fail to deliver shock due to a faulty circuit board

FDANov 3, 2004Nationwide• Access CardioSystems

Arc Fault Circuit Interrupters (Schneider) – Electrical Defect (2004)

Fire/Burn Risk

The recalled Square D QO® and Homeline® Arc Fault Interrupter circuit breakers are used with 15- and 20-amp branch circuits. They are required to be installed in bedroom circuits in accordance with the 2002 National Electrical Code. The recalled units were manufactured after March 1, 2004, and have a blue test button. The AFCI circuit breakers have one of the following date codes - CN, DN, EN, FN, GN, HN, or JN - stamped in red on the breaker label located just above the wiring terminal. The recalled units also have one of the following catalog numbers printed on a label on the front of the breaker: QO115AFI, QO115AFIC, QO120AFI, QO120AFIC, QOB115AFI, QOB120AFI, HOM115AFI, HOM115AFIC, HOM120AFI, HOM120AFIC, QO115VHAFI, QO120VHAFI, QOB115VHAFI, or QOB120VHAFI.

CPSCNov 3, 2004Nationwide• Schneider Electric North American Division, of Palatine, Ill.