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Abbott Laboratories MPG

Abbott Laboratories MPG Recalls

All product recalls associated with Abbott Laboratories MPG.

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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 24021–24040 of 25000 recalls

Abbott Laboratories MPG: ARCHITECT Folate Reagent Kit, list 6C12-20 ( 4 x 100 test...

concentrations for normal samples generated with current reagent lots of the ARCHITECT Folate assay are lower than data generated for the package insert.

FDAMar 11, 2005Nationwide• Abbott Laboratories MPG

Philips Medical Systems (Cleveland) Inc: Brilliance CT System, 40 channel configuration using vers...

When two product applications called Flip and Secondary Capture are used together, it is possible for image orientation labels to be incorrect.

FDAMar 11, 2005Nationwide• Philips Medical Systems (Cleveland) Inc

Philips Medical Systems (Cleveland) Inc: MX8000 Dual v.EXP CT scanner using Version 2.5 software.

When two product applications called Flip and Secondary Capture are used together, it is possible for image orientation labels to be incorrect.

1...1200 120112021203 1204...1250

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FDA

Mar 11, 2005

Nationwide

• Philips Medical Systems (Cleveland) Inc

Philips Medical Systems (Cleveland) Inc: Extended Brilliance Workspace using 1.x or 2.x software.

When two product applications called Flip and Secondary Capture are used together, it is possible for image orientation labels to be incorrect.

FDAMar 11, 2005Nationwide• Philips Medical Systems (Cleveland) Inc

Del Medical Systems Group: Tube Stand for the Dynarad Phantom Mobile X-Ray System; D...

The Phantom Portable X-Ray System Stand may have a suspect weld supporting the bracket holding the locking cylinder assembly. It the weld fails, the tubehead arm assembly could fall and contact the patient or operator.

FDAMar 10, 2005Nationwide• Del Medical Systems Group

Rear-Projection TV (JVC) – Technical Issue (2005)

Fire/Burn Risk

The recalled 52-inch and 61-inch JVC rear projection televisions were manufactured between May 2004 and November 2004. The televisions have the following model and serial numbers: HD-52Z575: 10980014 through 16980772HD-52Z575: 16986471 through 16989999HD-52Z585: 10980031 through 16981502HD-61Z575: 10980031 through 16982712 HD-61Z585: 10980031 through 16980942 The model and serial numbers can be found on the back of the television in the lower center portion of the unit. The JVC logo appears on the front of the television.

CPSCMar 9, 2005Nationwide• JVC Americas Corp., of Wayne, N.J.

Allen Medical Systems One Post Office Square: Allen A-91000 Shoulder Positioner

Shoulder positioner may break near the rail that attaches to the operating table

FDAMar 4, 2005Nationwide• Allen Medical Systems One Post Office Square

Trek Diagnostic Systems: Versa TREK REDOX 2 80 ml Anaerobic blood culture bottles,...

Blood culture bottles with an error in the bar code on the labels, were shipped.

FDAMar 4, 2005FL, GA, IL +15 more• Trek Diagnostic Systems

Radiometer America Inc: Radiance Data Management System Software Version 2.42 (St...

Software anomaly. Data generated by blood gas equipment did not correlate with data shown in the Radiance Data Management System.

FDAMar 2, 2005Nationwide• Radiometer America Inc

Brute Force ATV (Kawasaki) – Vehicle Defect (2005)

The recalled Kawasaki ATVs include the Brute Force™ 750 4x4i model, which was manufactured between April 26, 2004 and September 10, 2004. The ATVs come in red, green, yellow or camouflage, and have the words "Kawasaki" and "Brute Force" printed on each side of the vehicle's fuel tank. "VTwin 750" is printed on each side of the rear fenders, and "Kawasaki" is embossed on the front grille and rear mud flaps above the rear wheels.

CPSCFeb 28, 2005Nationwide• Kawasaki Motors Manufacturing Corp., USA of Lincoln, Neb.

Farm Teether Rattle (Tiffany) – Child Safety Risk (2005)

Laceration Risk

The recalled rattle is designed for children ages 3 months and up. The Farm Teether Rattle is a hollow, sterling silver ring approximately 3 inches in diameter with a bar across its center. The bar is attached to the interior of the ring at two points and has three farm animals (sheep, duck and cow) and two beads that rotate on the bar. Small plastic beads inside the ring rattle when the product is shaken. Inscribed on the rattle is "© 2002 TIFFANY & CO. 925."

CPSCFeb 25, 2005Nationwide• New England Sterling of Attleboro, Mass., for Tiffany and Company of New York, N.Y.

Dishwasher (Whirlpool) – Electrical Malfunction (2005)

Fire/Burn Risk

The recalled products are Whirlpool® brand and Kenmore® brand (made by Whirlpool Corporation) under-the-counter, plastic tall tub dishwashers. The dishwashers come with black, white, biscuit, or stainless front panels. They have the following model and serial numbers located inside the tub on a tag near the left side of the door opening: Brand Product Model Number Begins With Serial Number Range Whirlpool® Under-the-counter plastic tall tub dishwashers DU1, DUL, GU1, GU2, GU6 FR2200000 to FR2499999 Kenmore® Under-the-counter plastic tall tub dishwashers 665.143, 665.160, 665.163, 665.170, 665.173 FR2200000 to FR4599999 Not all dishwashers within the serial number range are included in the recall. Consumers should call Whirlpool to determine if their dishwasher is included in this recall.

CPSCFeb 25, 2005Nationwide• Whirlpool Corporation, of Benton Harbor, Mich.

Bioteque America Inc: Uterine Introducing Catheter 5F, 300 mm in length. The pr...

product is marketed without a 510(k)

FDAFeb 24, 2005IN, MI, OH• Bioteque America Inc

Proctor & Gamble Co: The product is a battery operated toothbrush. Spinbrush P...

The brushes may experience head breakage when insufficently rinsed after use and when used in combination with toothpastes containing a combination baking soda, peroxide, and sodium lauroyl sarcosinate.

FDAFeb 23, 2005Nationwide• Proctor & Gamble Co

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

FDAFeb 23, 2005Nationwide• Proctor & Gamble Co

Youth ATV (Kolpin Powersports) – Vehicle Safety Issue (2005)

The recall includes all of Kolpin Powersports' 2004 model year Youth ATVs purchased prior to November 24, 2004. The Youth ATVs are black with gray trim and have gray metallic and flame graphic decals. A "KOLPIN" decal is present on each side of the gas tank.

CPSCFeb 18, 2005Nationwide• Amstrong Industry Corporation, Taiwan, R.O.C.

Rope Candle (Gardener's Supply) – Fire Hazard (2005)

Fire/Burn Risk

The Rope Candle is a 21-foot coiled beeswax candle that feeds up to a scissors-like vise. The candle is lit above the vise. The candle is 7 inches tall and sits on an antiqued copper-finish holder.

CPSCFeb 18, 2005Nationwide• Zhongshan Zhongnam Candle Manufacturer Co., Ltd. of China

Dentsply Friadent Ceramed: PepGen P-15 Putty (0.5cc)

PepGen P-15 Putty kit was labeled with the incorrect expiration date.

FDAFeb 17, 2005Nationwide• Dentsply Friadent Ceramed

Toddler Drinking Cup (Charles Products) – Safety Concern (2005)

The toddler cups are made of clear plastic with two handles and have a blue lid with a spout for young children to drink from. The dome-shaped container inside the cup contains blue and clear liquid, along with two toy dolphins, which appear to be swimming in the liquid. "MAUI OCEAN CENTER" is written on the side of the cups.

CPSCFeb 17, 2005Nationwide• Charles Products, of Bethesda, Md.

Philips Medical Systems Sales & Service Region No. America: Easy Access Image Management System with CL.Net.

Failure to update correctly when re-transmitting an image from the modality.

FDAFeb 16, 2005Nationwide• Philips Medical Systems Sales & Service Region No. America