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Allen Medical Systems One Post Office Square

Allen Medical Systems One Post Office Square Recalls

All product recalls associated with Allen Medical Systems One Post Office Square.

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Recall Summary

Total Recalls

1000

Past Year

620

Class I (Serious)

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 10381–10400 of 10937 recalls

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

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."

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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.

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

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

Gas-Electric Heating Units (Trane/American Standard) – performance issue (2005)

Fire/Burn Risk

The recalled units include 2- through 5-ton Trane and American Standard heating and air conditioning packaged units. Affected units are combination gas heat and air conditioning systems installed outdoors only. Gas furnaces installed indoors are not included in this recall. The units have identification plates displaying the model number; serial number; and the year, month and day of manufacture. The plate is located on one end of the unit. The first four digits of all serial numbers indicate the year, fiscal week and day of manufacture. The recall includes: - All units with model numbers beginning with YCP or YCX and having serial numbers beginning with 3383 through 4475; - All units with model number beginning with YCY or YCZ and having serial numbers beginning with 4282 through 4475.

CPSCFeb 11, 2005Nationwide• Trane and American Standard, divisions of American Standard Inc., of Tyler, Texas

BISSELL Carpet Cleaner – handle defect (2005)

The recalled upright carpet deep cleaners have an open handgrip, a partially metal handle and come in a variety of colors. The word "BISSELL" is printed on the front of the unit. The recalled carpet cleaners have date codes beginning with 01, 02, 03 or 04 and include the following models: PowerLifter® Plus (model number 1620) PowerSteamer® ClearView® (model numbers 1692, 1692-1, 1692-R) Power Steamer® (model numbers 1685, 1693, 1693-R, 1693-W, 1694, 1694-1, 1694-R) Power Lifter® (model number 1694-3) Rubbermaid X-tra-Lift™ (model 9E00) The date codes and model numbers are printed on a label on the bottom of the unit. Cleaners with the model number and date codes listed above that are marked "Inspected" on or near the label are not included in the recall.

CPSCFeb 11, 2005Nationwide• BISSELL Homecare Inc., of Grand Rapids, Mich.

Philips Medical Systems Sales & Service Region No. America: Tomoscan

Potential for shift of reference lines.

FDAFeb 10, 2005Nationwide• Philips Medical Systems Sales & Service Region No. America

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Maximo DR, model 7278 Single Chamber Implantabl...

Medtronic marquis family of ICD and CRT-D devices having batteries manufactured prior to December 2003 that may experience rapid battery depletion due to a specific internal battery short mechanism. Once a short occurs, depletion can take place within a few hours to a few days, after which there is a complete loss of device function.

FDAFeb 9, 2005Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Maximo VR, model 7232 Single Chamber Implantabl...

FDAFeb 9, 2005Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Marquis DR, model 7274 Dual Chamber Implantable...

FDAFeb 9, 2005Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic InSync III Marquis, model 7279 Dual Chamber Imp...

FDAFeb 9, 2005Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic InSync Marquis, model 7277 Dual Chamber Implant...

FDAFeb 9, 2005Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Marquis VR, model 7230 Single Chamber Implantab...

FDAFeb 9, 2005Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic InSync II Marquis, model 7289 Dual Chamber Impl...

FDAFeb 9, 2005Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic InSync III Protect, model 7285 Dual Chamber Imp...

FDAFeb 9, 2005Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Decorative Candleholder (Horn Sing) – fire risk (2005)

Fire/Burn Risk

This recall involves moon, dolphin and fish themed candleholders. The decorative candleholders are about 9 inches tall with a metal bucket that sits suspended from a hook. A votive candle sits inside the bucket.

CPSCFeb 8, 2005Nationwide• Horn Sing Ind. Company Ltd., of Taipei, Taiwan

Varian Medical Systems Inc 3100 Hansen Way M/S E-210 Palo Alto CA 94304-1030: Varian brand Clinac 600C (CD, EX) and Portal Vison with D...

Treatment beam may not completely pause while device changes field shape; Potential for mistreatment could occur.

FDAFeb 4, 2005IN• Varian Medical Systems Inc 3100 Hansen Way M/S E-210 Palo Alto CA 94304-1030

Medtronic Emergency Response Systems, Inc.: LIFEPAK 500 AED.

Potential to not detect patients at the low end of the patient impedance range.

FDAFeb 3, 2005Nationwide• Medtronic Emergency Response Systems, Inc.