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Sammons Preston Rolyan, An Ability One Company

Sammons Preston Rolyan, An Ability One Company Recalls

All product recalls associated with Sammons Preston Rolyan, An Ability One Company.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

143

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 35301–35320 of 37665 recalls

Sammons Preston Rolyan, An Ability One Company: TM-300 Traction System; an Rx software driven device used...

The traction device may malfunction, producing oscillation and a jerking motion.

FDAJul 13, 2005Nationwide• Sammons Preston Rolyan, An Ability One Company

ArthroCare Corporation: ArthoCare Caps-Lock Cannula, polypropylene 70 mm cannula ...

Potential loss of product sterility due to breach of outer and inner seal packages, which may result in infection

FDAJul 12, 2005IL, IN, MD +8 more• ArthroCare Corporation

Medtronic Emergency Response Systems, Inc.: Hard shell carry case for the LIFEPAK 500 AED.

Some hard shell carry case for LIFEPAK 500 and LIFEPAK CR Plus automated external defibrillators may have blocked pressure vent which may make it difficult to open the case after a sudden decrease in altitude (such as in aircraft landng or mountain descent).

1...1764 176517661767 1768...1884

Page 1766 of 1884Next

FDA

Jul 12, 2005

Nationwide

• Medtronic Emergency Response Systems, Inc.

Nature's Bounty Multivitamins – Contamination Risk (2005)

The Nature's Bounty and Natural Wealth brand multivitamins have lot number 60835-06 written on the label. The recalled vitamins were sold in containers of 100 caplets. The containers are both clear with white caps. They are labeled "Nature's Bounty Multi-Day Multivitamin Plus Iron" or "Natural Wealth Daily Vitamin Plus Iron."

CPSCJul 12, 2005Nationwide• NBTY Inc., of Bohemia, N.Y.

Teleflex Medical: Rusch/MMG Urinary Catheterization System, 14 Fr; the sing...

There is a lack of assurance of sterility for parts of these lots of product.

FDAJul 11, 2005Nationwide• Teleflex Medical

Inprint Safe-Box (Perm-a-Store) – Security Flaw (2005)

Fire/Burn Risk

These silver Inprint™ safe-boxes are about 8 inches long, 6 inches wide and 12.5 inches high and have "INPRINT" written on the top of the safe. They have serial numbers 04470001 through 04470500 printed on the inside back panel near the battery tray.

CPSCJul 11, 2005Nationwide• Perm-A-Store, of Golden Valley, Minn.

JK Products & Services, Inc: SUN|DASH RADIUS 252 tanning system; 52 lamps, Ultraviolet...

The firm has tracked a systematic failure in the door cord on the Sun|Dash Radius 252 product line. In some instances when the door cord is installed with little or no slack outside the upper decor piece, the cord has been known to fail causing a short in the wiring at the pivot point in the cord.

FDAJul 8, 2005Nationwide• JK Products & Services, Inc

JK Products & Services, Inc: SUN|DASH RADIUS 252 tanning system; 52 lamps, Ultraviolet...

Class IIModerate

FDAJul 8, 2005Nationwide• JK Products & Services, Inc

Duo Tandem Stroller (Graco) – Potential Safety Defect (2005)

Laceration Risk

The recalled Duo Tandem strollers, manufactured between 1994 and 1999, have two seats, one seat in front and one seat in back. The strollers have a blue, white or green plastic and steel frame. They have four wheels in the front and two wheels in the rear. The cloth seats and tops have various colors and patterns. There is a label with the model and serial number on the stroller's frame. Only strollers with serial numbers and model numbers listed below are included in this recall. Graco Duo Tandem Model Numbers Serial Number Range 7950 7955 7960 7965 7970 7980 Between 01011994 and 12311999 7990 Between 01011996 and 10311998 The recalled MetroLite strollers, manufactured in 2000 and 2001, have a blue, gray or black plastic and steel frame. The cloth seat and top have various colors and patterns. The strollers have four wheels in the front and two wheels in the rear. These strollers were sold as a stand-alone stroller and also as part of a travel system that included an infant car seat/carrier and a base. The car seat/carrier is not affected. There is a label on the cross bar under the foot rest containing the model and serial number. Only strollers with serial numbers between 10012000 and 12312001 in the first 8 digits and the following model numbers are included in this recall. Graco MetroLite Model Numbers 6110DW 6114NGS 6110F3 7410CON 6111FKB 7413CML 6114HAV 7413MRN 6114JAM

CPSCJul 7, 2005Nationwide• Graco Children's Products Inc., of Exton, Pa.

Baxter Healthcare Corp. Rt.: Baxter Interlink System Y-Type Minivolume Extension Set, ...

Leaks and disconnection between the bifurcated Y-site and the set tubing may occur and result in underdelivery of medication, blood loss, and a breach of the sterile fluid pathway.

FDAJul 6, 2005AZ, GA, IL +5 more• Baxter Healthcare Corp. Rt.

Beckman Coulter Inc: Cytomics FC500 MPL with MXP Software versions 1.1 and 2.0

Software anomally. If the laser is shutdown or fluctuates outside of the specification limits, the software continues to run and will not indicate a laser failure, and could therefore cause erroneous results.

FDAJul 6, 2005Nationwide• Beckman Coulter Inc

Baxter Healthcare Corp. Rt.: Baxter Healthcare Corporation, Medication Delivery Divisi...

During an infusion in the 'Basal + PCA' or 'PCA only' modes, the SYNDEO pump may generate false Service Code 919 or Service Code 920, which will cause the pump to stop the infusion. Also, while attempting to turn on the device by pressing the On/Off key, the pump may not power up properly.

FDAJul 6, 2005Nationwide• Baxter Healthcare Corp. Rt.

Lawn Tractors (Tecumseh) – Mechanical Failure Risk (2005)

These lawn tractors have a 6-speed MST206-545C Peerless transaxle and a 17.5, 18, 18.5 or 19 horsepower engine. The recalled tractor and transaxle model number information is located below the tractor seat, and on the transaxle housing. The recalled transaxles have a date of manufacture code (DOM) between 4275 and 5047 followed by the letter "G", which can be found on the Transaxle ID Label. BRAND NAME COLOR HP RETAILER TRACTOR MODEL NO. Poulan Pro Black 18.5 Various Hardware Dealers 96012000300 Poulan Black 17.5 Various Hardware Dealers 96012001100 Poulan Pro Black 19 Various Hardware Dealers 96012001700 Poulan Pro Black 18.5 Various Hardware Dealers 96012002700 Southern States Red 17.5 Southern States Dealers 96012002200 Poulan Pro Black 18 The Home Depot 96016000200 Craftsman Gray 18 Orchard Supply Hardware 275390

CPSCJul 6, 2005Nationwide• Tecumseh Power Co., of Grafton, Wis.

Baxter Healthcare Corp. Rt.: Baxter Interlink System Minivolume Extension Set, product...

Leaks and disconnection between the bifurcated Y-site and the set tubing may occur and result in underdelivery of medication, blood loss, and a breach of the sterile fluid pathway.

FDAJul 6, 2005AZ, GA, IL +5 more• Baxter Healthcare Corp. Rt.

Guidant Cardiac Surgery: Aortic Cutter, single use device consisting of grip, cutt...

Laceration Risk

Incomplete or no aortotomy may occur with use of the aortic cutter on unaltered tissue, or incomplete aortotomy may result when the cutter is used on altered tissue. Use of the cutter on altered tissue has caused the aortic plug to not be captured by the device

FDAJul 5, 2005FL, MO, NE +1 more• Guidant Cardiac Surgery

Medtronic Neurosurgery: Medtronic Neurosurgery C/N 3805-014 Peelaway Introducer S...

Cracked hubs/handles and/or improper peeling of the sheath during use.

FDAJul 5, 2005Nationwide• Medtronic Neurosurgery

Becton Dickinson Medical Systems: DT-DL60-1 W/Bifurcated

Device could permit an over-infusion of IV solutions during pressure monitoring procedures.

FDAJul 1, 2005Nationwide• Becton Dickinson Medical Systems

ATV Wheels (HiPer Technology) – Potential Failure (2005)

The recalled 9-inch ATV aftermarket rear wheels have a model number of 0990 YHR. The rear wheels were manufactured from February 15, 2005 through May 2005. The recalled wheel can be used as the rear wheel on ATVs having the following bolt patterns: four bolts on a 110mm circle or four bolts on a 115mm circle. The center section of the wheel is made of aluminum and has eight bolt holes.

CPSCJul 1, 2005Nationwide• HiPer Technology Inc., of Lawrence, Kan.

Exercise Bench (Nautilus) – Structural Weakness (2005)

The Nautilus NT 1020 is a free-standing exercise bench typically used for free weight workouts. It is comprised of a white steel base with wheels on one end, with a black vinyl bench and back support. The fronts of both the white base and the black vinyl back support are stamped with the name "Nautilus." A tag affixed to the reverse side of the back support includes "Distributed by Nautilus/Schwinn Fitness Group Inc." and "Made in China." At the bottom of the product's base, near its wheels, is a sticker that includes the words "Production Date Code" and a 4-digit number. The first three digits of the date code identify the day and the fourth digit identifies the year in which the unit was built. Units included in this recall have Production Date Codes from year 2002 that run between code numbers 1952 and 3652, and Production Date Codes from year 2003 that run between code numbers 0013 and 1903. Benches that are white in color and do not have a Production Date Code sticker also are included in this recall.

CPSCJul 1, 2005Nationwide• Daytona Fitness Co., of Xiamen, China

Becton Dickinson Medical Systems: TAKHPQ60R continuous flow catheter.

Device could permit an over-infusion of IV solutions during pressure monitoring procedures.

FDAJul 1, 2005Nationwide• Becton Dickinson Medical Systems