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Aaron Medical Industries, Inc.

Aaron Medical Industries, Inc. Recalls

All product recalls associated with Aaron Medical Industries, Inc..

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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 24281–24300 of 25000 recalls

Aaron Medical Industries, Inc.: Battery-operated Cautery High Temperature, fine/Loop/ Va...

The cover caps on some of these cauteries are not properly engaged to prevent inadvertent activation.

FDAJun 29, 2004IN• Aaron Medical Industries, Inc.

Aaron Medical Industries, Inc.: Battery-operated Cautery Low Temperature, fine/elongated...

The cover caps on some of these cauteries are not properly engaged to prevent inadvertent activation.

FDAJun 29, 2004IN• Aaron Medical Industries, Inc.

Varian Medical Systems Inc: medical device and software systems

a malfunction in the software of the VARiS versions 6.2.27 and 6.2.35 which is used to set up radiation therapy devices which will reset parameters to null for future treatments if a patient receives treatment on a non-varian machine and a varian machine and a non-varian field is loaded in the treatment session.

FDA

1...1213 121412151216 1217...1250

Page 1215 of 1250Next

Jun 24, 2004

Nationwide

• Varian Medical Systems Inc

Rock 'N Roller Baby Stroller (Dorel Juvenile Group) – Seat Detachment Risk (2004)

The COSCO® "Rock 'N Roller" strollers involved have seats that can be removed from the stroller frame. The detached seat can function as a bassinet or be repositioned on the stroller frame facing front or back. The stroller has a dark blue or green metal frame with four wheels on the front and two wheels on the back. The side folding area of the frame has a white plastic cover that is labeled "Rock 'N Roller by Geoby COSCO®." There is a label on the back of the frame containing one of the following model numbers: "01-654, 01-622, 01-624, 01-646 or 01-656." The seat cover is usually a dark blue or green printed fabric with "COSCO® A Dorel Company" printed on the footrest.

CPSCJun 23, 2004Nationwide• Dorel Juvenile Group USA, of Columbus, Ind.

Wheelbarrows (Ames) – Wheel Assembly Defect (2004)

Laceration Risk

The wheel assemblies on these wheelbarrows have a black plastic rim and have an approximately 14-inch diameter wheel. They have red, green, or orange tubs or trays made of steel or plastic and were sold under the brand names "Easy Roller," "Homeowner," "Mustang," or "Thoroughbred." The brand name was printed on the label attached to the tray at the time of purchase. Wheelbarrows with metal wheel assemblies are not part of this recall. No "True Temper" or "Jackson" wheelbarrow is part of this recall. In addition to the free replacement wheel assembly and free gardening tool incentive, the company is conducting the recall campaign with new measures to reach home gardeners who are the primary users of these recalled wheelbarrows. These new measures include placing ads in gardening publications, providing recall information to editors and webmasters of specialty gardening magazines and websites, and providing new point-of-sale posters to retailers.

CPSCJun 23, 2004Nationwide• O. Ames, a predecessor company of Ames True Temper Inc., of Camp Hill, Pa.

North Coast Medi-Tek Inc: E-Z-EM brand, Basic biopsy tray, catalog no. 4125.

Product contains the incorrect lot number.

FDAJun 23, 2004NY• North Coast Medi-Tek Inc

Argon Medical Devices, Inc: Argon Medical Devices, Vesseloops, Blue Maxi, Two Latex f...

Inadequate closure compromising sterility.

FDAJun 22, 2004CA, IN, MO +7 more• Argon Medical Devices, Inc

Basic Editions Girls' Rompers (Kmart) – Design Safety Issue (2004)

Choking Hazard

The recalled rompers are pink and white gingham with pink buttons and crocheted cherry-shape tassels on the pocket and green and white gingham bows on the trim of the leg openings. The rompers were sold in infant sizes 12 months to 24 months and toddler sizes 2T to 5T. "MADE IN/HECHO EN BANGLADESH" and "basic EDITIONS®" is printed on a label inside the neck of the garment.

CPSCJun 22, 2004Nationwide• Kmart Corporation, of Troy, Mich.

Toddler Doll Family Sets (Lakeshore Learning) – Potential Hazard (2004)

Choking Hazard

The recall involves Toddler Doll Family sets sold with four figurines, a mom, dad, brother and sister. The 4-inch-tall dolls have a wooden head, arms and feet. The body is constructed of wire, which makes the doll adjustable. Each doll has yarn hair and is dressed in various colored outfits.

CPSCJun 22, 2004Nationwide• Lakeshore Learning Materials, of Carson, Calif.

Children's Swimsuit Cover-ups (Samara Brothers) – Unspecified Safety Concern (2004)

Choking Hazard

The recalled cover-ups were sold in various colors for boys and girls. Cover-ups were sold separately or as part of a swimsuit set. The cover-ups were sold under the brand names "Samara" and "Carter's," in sizes ranging from 3 to 24 months, 2T to 4T and 4X to 6X. On the short-sleeved cover-up are various patches depicting beach and swim-related themes. The name "Samara" or "Carter's" is printed on the garment-care tag, along with the size.

CPSCJun 22, 2004Nationwide• Samara Brothers Inc., of Edison, N.J.

Toshiba American Med Sys Inc: Digital Radiography System, model DFP-8000D

Defect in the mirroring unit.

FDAJun 18, 2004Nationwide• Toshiba American Med Sys Inc

Advance Medical Designs Inc: Advance Medical''s, The Closed Camera System, 9'' x 96'' ...

The product may come apart when excessive force is applied to the coupler.

FDAJun 18, 2004Nationwide• Advance Medical Designs Inc

Rita Medical Systems: Dispersive Electrodes packaged in an 8x10 plastic container.

Inaccurate temperature readings may be displayed by the device, actual temperature could be 2.5-3 degrees C higher than displayed.

FDAJun 16, 2004Nationwide• Rita Medical Systems

Grocery Frozen Food Case Heaters (Electro-Heat) – Electrical Risk (2004)

The recalled defrost heater was used in Tyler's "wide island" frozen food end cap cases in grocery stores. The recalled defrost heaters (which are not visible to consumers) are Electro-Heat Defrost Heater Model 51957100. The Tyler wide island frozen food end cap cases with the recalled heaters are models NCE, NFE, NGE, NCGE, NFJEA, NCJEA, NCJGEA and NFJGEA. The model and serial number is located on the data plate, which is on the front inner panel of the case.

CPSCJun 16, 2004Nationwide• Electro-Heat Inc., of Allegan, Mich.

Ossur North America Inc: VSP Shock Module (as part of a prosthetic foot).

Flawed shock module might cause breakage causing patient to fall.

FDAJun 15, 2004Nationwide• Ossur North America Inc

Reedy Quasar Pro Battery Charger (Associated Electrics) – Charging Malfunction (2004)

The recalled #611 Quasar Pro Chargers were manufactured from February 2002 through February 2004. The gray charger box has words "Quasar Pro" printed in yellow on the front and shows a display of "QUASAR PRO VERSION 1.0" when first turned on. The recalled chargers either have no barcode label on the underside or a barcode label with the numbers "611" or "611A".

CPSCJun 15, 2004Nationwide• Associated Electrics Inc., of Costa Mesa, Calif.

Wooden Organ Bench (Allen Organ) – Structural Integrity Concern (2004)

The recalled wooden organ bench is sold primarily to churches and theaters as part of a package that also includes an organ, console, pedal board, and speaker cabinets. A very small number of the wooden organ benches were sold separately. The wooden organ bench measures 26 inches high, 12 inches wide, and 48 inches long. The benches are made of oak, red oak, and walnut colored wood.

CPSCJun 14, 2004Nationwide• Allen Organ Company of Macungie, Penn.

Thomas Medical Products Inc: SafeSheath CSG (Coronary Sinus Guide) KR-90.09 and CSG (C...

Degradation of sheath due to excessive exposure to (ultra violet) fluorescent light.

FDAJun 11, 2004CA, IN, OR +1 more• Thomas Medical Products Inc

Thomas Medical Products Inc: Safe Sheath CSG (Coronary Sinus Guide)-90.09; CSG (Corona...

Degradation of sheath due to excessive exposure to (ultra violet) fluorescent light.

FDAJun 11, 2004CA, IN, OR +1 more• Thomas Medical Products Inc

Thomas Medical Products Inc: SafeSheath CSG (Coronary Sheath Guide) Multisite (MSP)-00...

Degradation of sheath due to excessive exposure to (ultra violet) fluorescent light.

FDAJun 11, 2004CA, IN, OR +1 more• Thomas Medical Products Inc