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Medstone International Inc

Medstone International Inc Recalls

All product recalls associated with Medstone International Inc.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

145

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 36741–36760 of 37661 recalls

Medstone International Inc: URO PRO Plus Digital Urology Imaging System

X-ray tube arm and collimator fell and fractured patient's ribs.

FDAAug 11, 2003CA, NV, NM +1 more• Medstone International Inc

Harvard Clinical Technology: Software Versions V1.2R,or earlier for the Harvard 2, Dua...

Under specific sequence conditions, the unit may apper to be infusing, but is not

FDAAug 11, 2003Nationwide• Harvard Clinical Technology

Philips Medical Systems Sales & Service Region No. America: Diagnost 94

Potential for table to move by itself

FDAAug 10, 2003Nationwide• Philips Medical Systems Sales & Service Region No. America

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Philips Medical Systems Sales & Service Region No. America: Diagnost 97

Potential for table to move by itself

FDAAug 10, 2003Nationwide• Philips Medical Systems Sales & Service Region No. America

Philips Medical Systems Sales & Service Region No. America: Diagnost 96

Potential for table to move by itself

FDAAug 10, 2003Nationwide• Philips Medical Systems Sales & Service Region No. America

Terumo Cardiovascular Systems Corp: Sarns brand Retrograde Cardioplegia Cannula, 17 Fr, steer...

Product is labeled as sterile, but inadequate package seal results in lack of assurance of sterility.

FDAAug 8, 2003Nationwide• Terumo Cardiovascular Systems Corp

Bard Endoscopic Technologies: Bard Ponsky PEG Safety System ''Pull'' Reorder Number: 00...

Mislabeled kit: Prefilled Lidocaine syringe is labeled 'sterile fluid path only', outer label states kit content is sterile

FDAAug 4, 2003Nationwide• Bard Endoscopic Technologies

Bard Endoscopic Technologies: Bard PEG Safety System ''Guidewire'' Reorder Number: 000930

Mislabeled kit: Prefilled Lidocaine syringe is labeled 'sterile fluid path only', outer label states kit content is sterile

FDAAug 4, 2003Nationwide• Bard Endoscopic Technologies

Stryker Howmedica Osteonics: T2 Tibia Nail, Standard 9 x 300 mm, T2 Tibia System, Cat...

The device does not have an oblong hole for dynamic locking as required.

FDAAug 4, 2003CA, GA, IN +3 more• Stryker Howmedica Osteonics

Exactech, Inc.: Exactech Tibial Augmentation Block Trial Size 0, Exactech...

Misalignment of the fixation holes between the tibial augment block trials and the corresponding tibial tray trials and trapezoid tray trials. The misalignment of the pin fixation holes only creates an issue when augmentation is used.

FDAAug 1, 2003Nationwide• Exactech, Inc.

Plus Orthopedics: 17 mm thickness only of a polyethelene insert, which sits...

Plastic insert over articular surface of knee joint replacement may become dislodged.

FDAAug 1, 2003AZ, ID, TX• Plus Orthopedics

Kiddy Sling Chair (Wal-Mart) – Child Seating Hazard (2003)

Choking Hazard

The chairs are steel outdoor chairs with a white frame and a pink or blue sling fabric seat and back. The chairs measure about 9.5 inches in height. The seats have two small plastic covers located behind the back of the seat and two covers under the seat.

CPSCJul 31, 2003Nationwide• Wal-Mart Stores, Inc., of Bentonville, Ark.

Bobbie Bear Stacking Rings (International Playthings) – Toy Design Risk (2003)

Choking Hazard

The recalled Bobbie Bear Stacking Rings have a blue and orange rounded bottom, two multicolored stacking rings, and an orange plastic bear head topper. The toy can be spun like a top and makes a rattling sound when shaken. The toy is designed for children ages 6-24 months and has a model number of E00421, which can be found on the packaging.

CPSCJul 31, 2003Nationwide• International Playthings Inc., of Parsippany, N.J.

Hedstrom Trampolines (Hedstrom Corp) – Size Safety Concern (2003)

These are 12-foot, 13-foot, and 14-foot trampolines, which were sold separately, and also banded together with safety enclosures. They were sold under the brand names Hedstrom and NBF. The brand name is written on the warning labels found on the products. The recalled trampolines have model numbers 10136, 101366, 101442, 10146, 102369, 102949, 10321, 103217 or 10381. They also have four-digit date codes ranging from 0403 through 2103 with the last two digits always being 03. Model I.D. labels showing the model number and date code are located on one of the frame rail legs on the trampoline.

CPSCJul 31, 2003Nationwide• Hedstrom Corp., of Bedford, Pa.

Solenoid Voltage Testers (Ideal Industries) – Model Number Issue (2003)

Fire/Burn Risk

These are Ideal voltage and voltage/continuity testers with model numbers 61-065, 61-066, 61-067, 61-076, 61-079, and 61-080. "IDEAL" and the model number are located on the front of the tester. The tester body is yellow. The wire leads have one black and one red test probe. Recalled units were manufactured between November 1999 and May 2002. Contact Ideal to determine if your electrical tester is included in this recall.

CPSCJul 31, 2003Nationwide• Ideal Industries Inc., of Sycamore, Ill.

Exactech, Inc.: Exactech Tibial Offset Bushing (sizes 1, 2, 3, 4, & 5) Ca...

The alpha and beta markings on the offset tibial bushings are in a location that would lead to the improper selection of an offset tibial tray.

FDAJul 30, 2003HI, IN, ME +2 more• Exactech, Inc.

American Medical Systems: Monarc Subfascial Hammock With Tensioning Suture, Product...

Insertion needles from the former version of the product were packaged with the new sling with dilator that is different than the old version and not compatible with the old needles.

FDAJul 28, 2003Nationwide• American Medical Systems

Datascope Collagen Products Division: VasoSeal ES, Extravascular Security Vascular Closure Devi...

Kits are missing the temporary arteriotomy locator (TAL) from the blister package.

FDAJul 28, 2003Nationwide• Datascope Collagen Products Division

Misys Healthcare Systems: Calculator/ Data Processing Module for Clinical Use

Software Design Defect. Under certain conditions, results are removed.

FDAJul 24, 2003Nationwide• Misys Healthcare Systems

Misys Healthcare Systems: Calculator/ Data Processing Module for Clinical Use

Software Defect. Data used in the diagnosis and or treatment of a patient's illness are missing from the patient result report.

FDAJul 23, 2003Nationwide• Misys Healthcare Systems