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
/
Icotec Ag Industriestrasse 12 Altstatten Sg Switzerland

Icotec Ag Industriestrasse 12 Altstatten Sg Switzerland Recalls

All product recalls associated with Icotec Ag Industriestrasse 12 Altstatten Sg Switzerland.

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 3021–3040 of 21320 recalls

VADER Pedicle System (Icotec) – Loose Nut Screws (2023)

icotec has received notification of one revision that had to be carried out because nut screws had become loose. During the investigation of the device involved, it was detected that the torque limiting function of the wrench used to tighten the nut screws during implantation was not functioning correctly. Due to the malfunction, the nut screws may not have been tightened sufficiently.

Moderate

FDANov 28, 2023AZ, CA, CO +7 more• Icotec Ag Industriestrasse 12 Altstatten Sg Switzerland

EDS 3 CSF Drainage System (Natus) – Sterility Concern (2023)

Sterility assurance cannot be guaranteed for external drainage systems due to incomplete bioburden testing.

Moderate

FDANov 28, 2023Nationwide• Natus Medical Incorporated

Percutaneous Pin (Medtronic) – Potential Fitting Issue (2023)

Laceration Risk

Their is the potential that the percutaneous pin may have a cross-pin that may render the pin unable to fit into tap cap, or too tight to remove.

1...150 151152153 154...1066

Page 152 of 1066Next

Moderate

FDANov 28, 2023Nationwide• Medtronic Navigation, Inc.

External Drainage Collection Bag (Natus) – Sterility Concern (2023)

Sterility assurance cannot be guaranteed for external drainage systems due to incomplete bioburden testing.

Moderate

FDANov 28, 2023Nationwide• Natus Medical Incorporated

CareEvent Monitor (Philips) – Push Notification Failure (2023)

Push notifications may fail to send to the user under certain conditions. This could potentially result in patient harm due to delay in detection of a change in patient condition.

Moderate

FDANov 28, 2023Nationwide• Philips North America

Tank Hose Assembly (AtriCure) – Incorrect Supplier (2023)

AtriCure has identified certain lots of tank hose assemblies where a second-tier supplier provided incorrect tank hose assemblies. These tank hose assemblies were provided with an outer sheathing that does not have required pin perforations and the inner tube of the hose is not the correct material.

Moderate

FDANov 28, 2023Nationwide• AtriCure, Inc.

Percutaneous Pin (Medtronic) – Potential Fitting Issue (2023)

Laceration Risk

Their is the potential that the percutaneous pin may have a cross-pin that may render the pin unable to fit into tap cap, or too tight to remove.

Moderate

FDANov 28, 2023Nationwide• Medtronic Navigation, Inc.

Cryo Module Accessories (AtriCure) – Incorrect Supplier (2023)

Moderate

FDANov 28, 2023Nationwide• AtriCure, Inc.

Trilogy Evo Respirator – Missing Contraindication Statement (2023)

The following was missing from the Contraindications Statement: The AVAPS-AE therapy mode is contraindicated for invasive use and patients less than 10 kg. The AVAPS feature is contraindicated for patients less than 10 kg. Potential harms if devices are used on contraindicated patients include barotrauma, hypoventilation/hypercapnia, and rebreathing of excessive CO2.

Moderate

FDANov 27, 2023Nationwide• Philips Respironics, Inc.

BIOFIRE Gastrointestinal Panel – False Negative Results (2023)

A manufacturing event may contribute to elevated rates of false negative results while using gastrointestinal panel and respiratory panel, which could lead to inappropriate antibiotic treatment, no treatment, delay of treatment, and may provide false assurance to someone with a true infection, delayed identification of an outbreak, and may result in additional transmission.

Moderate

FDANov 27, 2023CA, CT, FL +13 more• BioFire Diagnostics, LLC

VITROS Anti-HBs Quantitative Reagent – Calibration Failures (2023)

Affected lots may experience increased calibration failures or an increase in falsely elevated results.

Moderate

FDANov 27, 2023Nationwide• Ortho-Clinical Diagnostics, Inc.

BIOFIRE Respiratory Panel – False Negative Results (2023)

Moderate

FDANov 27, 2023CA, CT, FL +13 more• BioFire Diagnostics, LLC

Whole Cantaloupe (Pacific Trellis) – Salmonella (2023)

Salmonella

Class IHigh

FDANov 24, 2023CA, IL, OK +2 more• PACIFIC TRELLIS FRUIT, LLC

Fujifilm Mobile X-Ray System – Incorrect Default Settings (2023)

When the key switch is turned on, the exposure conditions are set to the default values (85kV, 1.6 mAs, approx. 0.13mGy@ SID 1m) intended for adult chest imaging. In addition, if exposure conditions are set from the console while the key switch is off, the set exposure conditions will not be reflected.

Moderate

FDANov 23, 2023Nationwide• FUJIFILM Healthcare Americas Corporation

Micro Bird G5 School Bus – Critical Fastener Defect (2023)

Corp. Mirco Bird, Inc. (Micro Bird) is recalling certain 2006-2008 G5, 2010-2012 G5, 2014-2015 G5, and 2020-2021 G5 school buses equipped with transversal wheelchair track anchorages. The wheelchair track anchorages may not sufficiently secure a wheelchair and detach during a crash. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 222, "School Bus Passenger Seating and Crash Protection."

High

NHTSANov 23, 2023Nationwide• MICRO BIRD

SANDIMMUNE Oral Solution (Novartis) – Crystallization Risk (2023)

Crystallization: bottles of Sandimmune Oral Solution were determined to contain crystals

Class IHigh

FDANov 22, 2023Nationwide• Novartis Pharmaceuticals Corporation

Penicillamine Tablets (Lupin) – Dissolution Failure (2023)

Failed Dissolution Specifications

Class IIModerate

FDANov 22, 2023Nationwide• Lupin Pharmaceuticals Inc.

buPROPion Tablets (Sun Pharmaceutical) – Failed Dissolution (2023)

Failed Dissolution Specifications

Class IIILow

FDANov 22, 2023Nationwide• SUN PHARMACEUTICAL INDUSTRIES INC

TING Athlete's Foot Spray (Insight Pharmaceuticals) – Benzene Contamination (2023)

Chemical Contamination; presence of benzene.

Class IHigh

FDANov 22, 2023Nationwide• Insight Pharmaceuticals Corporation

QMS Tacrolimus Calibrators – Improper Storage (2023)

Ortho-Clinical Diagnostics, Inc. is recalling QMS Tacrolimus Calibrators, Lot 74859619 expiry date: May 11, 2024, due to improper storage that is expected to degrade the quality of the calibrator and render it unsuitable for use. Use of the affected lot may results in erroneous calibration results, causing delay in testing.

Moderate

FDANov 21, 2023FL, IL, IN +3 more• Ortho-Clinical Diagnostics, Inc.