Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Plus Orthopedics USA

Plus Orthopedics USA Recalls

All product recalls associated with Plus Orthopedics USA.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

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 20981–21000 of 21319 recalls

Plus Orthopedics USA: Plus Orthopedics Gliding Nail 17mm proximal / 11mm distal...

The device was produced without the required distal locking hole

FDAJun 30, 2003Nationwide• Plus Orthopedics USA

Power Medical Interventions: SurgASSIST System. Circular Stapler DLU 29 mm (product co...

latching mechanism failure

FDAJun 30, 2003Nationwide• Power Medical Interventions

Depuy Orthopaedics, Inc.: ProVision Hytrel Elastomer Hood; product 5431-05-000.

Lack of assurance of sterility, due to the possibility of an incomplete package seal.

FDAJun 27, 2003Nationwide• Depuy Orthopaedics, Inc.

1...1048 104910501051 1052...1066

Page 1050 of 1066Next

Depuy Orthopaedics, Inc.: ProVision Hytrel Universal Hood/Gown; product 5431-31-000

Lack of assurance of sterility, due to the possibility of an incomplete package seal.

FDAJun 27, 2003Nationwide• Depuy Orthopaedics, Inc.

Philips Medical Systems: Easy Access Software releases 1.1, 5.2, 6.2 & 7.2

If DICOM fields for body part, description or accession number are changed, change won't update on the EasyWeb client or hospital systems.

FDAJun 27, 2003Nationwide• Philips Medical Systems

Depuy Orthopaedics, Inc.: ProVision Barrier Universal Hood/Gown; product 5431-33-000

Lack of assurance of sterility, due to the possibility of an incomplete package seal.

FDAJun 27, 2003Nationwide• Depuy Orthopaedics, Inc.

Depuy Orthopaedics, Inc.: ProVision Disposable Hood; product 5431-50-000

Lack of assurance of sterility, due to the possibility of an incomplete package seal.

FDAJun 27, 2003Nationwide• Depuy Orthopaedics, Inc.

Roche Diagnostics Corp.: MagNA Pure LC Instrument; Catalog number 2236931.

A software bug in version 3.0 may result in prolonged mixing time, evaporation of elution volume and biased sample results for various protocols.

FDAJun 26, 2003Nationwide• Roche Diagnostics Corp.

Boston Scientific Corporation: Wallstent Enteral Endoprothesis with Unistep Plus Deliver...

Mislabeled: Product is labeled as a 20 mm X 90 mm, but is actually a 22 mm X 60 mm

FDAJun 26, 2003CO, FL, IL +4 more• Boston Scientific Corporation

Ski-Doo Snowmobiles (Bombardier) – Vehicle Safety Issue (2003)

Laceration Risk

The recalled snowmobiles are 2-tone blue or all black. The name of the engine is written on the hood: Rotax 4-TEC V-1000 or Rotax 2-TEC 800 SDI.

CPSCJun 24, 2003Nationwide• Bombardier Motor Corporation of America, of Grant, Fla.

Boston Scientific Corporation: Fibered Platinum Coil, 0.035 Type, 4 mm x 30 mm Catalog...

Product 's Outer box label may not match pouch label: a 4mm x 30 mm coil may be labeled as a 9 mm x 60 mm or vice versa

FDAJun 23, 2003Nationwide• Boston Scientific Corporation

Zoll Medical Corporation: Zoll M Series External Defibrillator

Defibrillator may fail to charge or hold its charge above energies of 75 joules

FDAJun 23, 2003Nationwide• Zoll Medical Corporation

Bayer HealthCare LLC, Diagnostics Div: Clinitek 50 Urine Chemistry Analyzer; Product codes 6509C...

Analyzer will produce erroneous results due to missing grounding strap.

FDAJun 19, 2003Nationwide• Bayer HealthCare LLC, Diagnostics Div

Crib Mobile Toys (Fisher-Price) – Remote Control Hazard (2003)

Fire/Burn Risk

These are Sparkling Symphony™ Mobile crib toys that attach to the crib side rail and play music and lights that are activated by remote control. Four star and moon characters are suspended from the mobile, which turns. The recalled toys have model number 71985 found on both the lower arm of the mobile and the back of the remote control. The Fisher-Price logo appears at the top of the upper arm, over the silver decoration. The recalled mobiles were manufactured from October 1999 through November 2000. A date code is located on the upper arm of the mobile and on the back of the remote control. Consumers should contact Fisher Price with their date code to determine if their mobile is part of the recall.

CPSCJun 19, 2003Nationwide• Fisher-Price, of East Aurora, N.Y.

LMA North America Inc: LMA- Unique Laryngeal Mask Airway Size 4, Catalog No. 1...

Sterility cannot be assured

FDAJun 18, 2003Nationwide• LMA North America Inc

Sanarus Medical Inc: Sanarus Visica Treatment System (disposable), Model/Produ...

Corrosion in stainless steel device shaft that allows Argon gas to escape from device during a cryoablation procedure.

FDAJun 16, 2003Nationwide• Sanarus Medical Inc

Ballard Medical Products: Kimberly-Clark / Ballard TRACH-CARE* MAC (Multi Access Ca...

Incorrect plug was included in the multi access catheter pkg. When inserted in the 'Y' it may disengage, allowing a leak of ventilator gases.

FDAJun 13, 2003Nationwide• Ballard Medical Products

Ohmeda Medical, A division of Datex-Ohmeda, Inc.: Servo Controlled Oxygen System for Ohmeda''s Medical Gira...

Firm's received complaints of medical device malfunction affecting instrument's calibration and alarm systems.

FDAJun 13, 2003Nationwide• Ohmeda Medical, A division of Datex-Ohmeda, Inc.

Zeus Scientific Inc: Cytomegalovirus (CMV) IgG ELISA Test System, In-Vitro Dia...

The Calibrator included within the kit may be losing reactivity.

FDAJun 12, 2003Nationwide• Zeus Scientific Inc

MedAmicus, Inc: AngioDynamics 15F EmboSafe Valved Peelable Introducer, 5 ...

Stability testing, after accelerated aging of the device, showed that the handle of device did not meet strength specifications.

FDAJun 6, 2003GA, IN, MO +3 more• MedAmicus, Inc