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
/
Concentric Medical Inc

Concentric Medical Inc Recalls

All product recalls associated with Concentric Medical Inc.

Get alerts for this brand

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 32081–32100 of 37665 recalls

Concentric Medical Inc: Concentric 7F Balloon Guide Catheter (percutaneous cathet...

Product malfunction-- hub may leak at connection to the shaft due to insufficient adhesive curing.

FDAFeb 27, 2009AL, FL, GA +11 more• Concentric Medical Inc

ArjoHuntleigh: Flite Clip Slings; patient specific disposable sling; Man...

If the sling clips are not applied or are applied incorrectly, there is the potential for the patient to fall, resulting in injury to both the patient and/or the caregiver.

FDAFeb 26, 2009Nationwide• ArjoHuntleigh

ArjoHuntleigh: Passive Clip Slings; washable sling; Manufactured in Belg...

If the sling clips are not applied or are applied incorrectly, there is the potential for the patient to fall, resulting in injury to both the patient and/or the caregiver.

FDAFeb 26, 2009Nationwide

1...1603 160416051606 1607...1884

Page 1605 of 1884Next

• ArjoHuntleigh

Abbott Laboratories: ARCHITECT Reaction Vessel, 2000 units per carton; for in ...

Abbott has had an increase in complaints due to the receipt of error code 1006 (unable to process test, background read failure), error code 1007 (unable to process test, activated read failure) and incorrect results when using these lots of ARCHITECT Reaction Vessels.

FDAFeb 26, 2009Nationwide• Abbott Laboratories

Medtronic Cardiovascular Revascularization & Surgical Therap: Medtronic, Transfer Spike, Blood Processing Accessory, RE...

Sterility may be compromised. Non-vented caps that connect to the 3-way stopcock attached to the transfer spike could prevent Ethylene Oxide from contacting the inside surfaces of the stopcock during sterilization, leading to a potentially non-sterile product. Use of the product may cause serious health consequences from potential sepsis/infection and the associated remote risk of death.

FDAFeb 25, 2009IN, MN• Medtronic Cardiovascular Revascularization & Surgical Therap

Air Rifles (Air Venturi) – unexpected firing (2009)

Fire/Burn Risk

This recall involves model 909S Sam Yang .45 caliber rifles shipped to consumers after July 1, 2008. The rifle is a precharged pneumatic air rifle, powered by compressed air.

CPSCFeb 24, 2009Nationwide• Sam Yang Precision Industrial, of South Korea

Scuba Diving Hoses (Ambient Pressure) – drowning risk (2009)

The crimped hoses are used to carry the air supply in the re-breathing diving system. The hoses were sold on three re-breathing models: Inspiration, Evolution and Evolution Plus. Hoses with a smooth (uncrimped) collar and with the model numbers listed below are included in the recall: AP300/15 ADV Supply Hose RB20/03 Oxygen Injection Hose EV20/03 Oxygen Injection Hose RB20/10 Buzzer Hose EV11A/1 Vision Handset Hose RB11A/1 Classic Handset Hose RB11/B Handset Hose AP300/10 ADV Hose AP300/38 ADV Hose Hoses with eight flats on the hose collar have been crimped and are not included in the recall.

CPSCFeb 24, 2009Nationwide• Ambient Pressure Diving Ltd., of Helston, Cornwall, United Kingdom

GE Healthcare: GE Healthcare ApexPro Telemetry System for mobile patient...

Intermittent or continuous loss of patient monitoring.

FDAFeb 24, 2009Nationwide• GE Healthcare

Sybron Dental Specialties: Sealapex Express (Part Number: 33639), root canal filling...

Sybron Dental Specialties is initiating a recall on the Sealapex Xpress due to the presence of crystals in the catalyst. This crystallization may affect proper canal filling by preventing Gutta Percha Points from reaching the bottom of the root canal which may lead to an inadequate seal.

FDAFeb 23, 2009Nationwide• Sybron Dental Specialties

Abbott Point of Care Inc.: i-STAT EG7+ Cartridge; pH, PCO, PO, Na , K, iCa, Hct. Tes...

Equipment problem: i-STAT cartridges were not properly sealed as the packaging system jammed, causing compromised seals.

FDAFeb 23, 2009Nationwide• Abbott Point of Care Inc.

Abbott Point of Care Inc.: i-STAT G3+ Cartridge; pH, PCO, PO. HCO2, TCO2, BE sO2; Te...

Equipment problem: i-STAT cartridges were not properly sealed as the packaging system jammed, causing compromised seals.

FDAFeb 23, 2009Nationwide• Abbott Point of Care Inc.

Sybron Dental Specialties: Herculite Ultra (Part Number 34333), dental composite res...

Sybron Dental Specialties is initiating a field correction on the Herculite Ultra, a dental composite restorative material, due to a mistake in the directions for use located in the Herculite technique card.

FDAFeb 23, 2009Nationwide• Sybron Dental Specialties

Abbott Laboratories: Abbott AxSYM Cancer Assay Disk Version 5.0, for in vitro ...

The AxSYM Cancer Assay Disk (LN 3D50-05 version 5.0) contains an AxSYM AFP assay file where the Low Concentration flag for the AFP 1:101 automated dilution protocol the instrument to report results between 0 ng/mL and 0.4 ng/mL (40.4 ng/mL accounting for the 1:101 dilution). The sensitivity of the assay is 0.4 ng/mL.

FDAFeb 20, 2009Nationwide• Abbott Laboratories

Polymer Technology Systems, Inc.: PTS Panels CHOL+HDL Panel test strips for professional us...

Extended expiration date; the product expired on February 12, 2009 but was labeled with a April 4, 2009 expiration date.

FDAFeb 20, 2009Nationwide• Polymer Technology Systems, Inc.

Wright Medical Technology Inc: Screwdriver for 3.5mm Screws, DARCO system, instrument fo...

The package insert lists 3 sterilization procedures, 2 of which are not validated. Pre-vacuum steam sterilization is validated.

FDAFeb 19, 2009Nationwide• Wright Medical Technology Inc

Ge Healthcare: GE Healthcare Fluorostar 7900 Mobile Fluoroscopy System

The alarm timer is reset after each exposure and therefore never reaches the five minute alarm state unless one exposure exceeds 5 minutes in duration.

FDAFeb 19, 2009Nationwide• Ge Healthcare

Philips Medical Systems (Cleveland) Inc: TumorLoc software application, Software Versions: 23.1.1,...

A software anomaly in the TumorLoc software for the firm's Brilliance CT scanners was discovered. The same software anomaly was subsequently determined to be present in the firm's GEMINI PET/CT units. The software defect results in a the potential for data to be lost during reconstruction of images in which slices can either be discarded, or interleaved based upon their series ID.

FDAFeb 19, 2009Nationwide• Philips Medical Systems (Cleveland) Inc

Beckman Coulter Inc.: SYNCHRON Gentamicin (GEN) Reagent GEN reagent, when used ...

The reagent produces false low test results. Beckman Coulter has confirmed low recovery of values at the low end of the therapeutic range (<1.5 ug/mL, <3.13 umol/L) with SYNCHRON Systems Gentamicin Reagent (GEN) lot M804552. A false low result can cause a patient to receive more medication than necessary.

FDAFeb 19, 2009AL, AZ, AR +42 more• Beckman Coulter Inc.

General Compound Bows (BowTech) – breaking risk (2009)

This recall involves the "The General" compound bows hunting and target models with draw weights of 60 and 70 pounds that do not have a collet (see illustration) in the limb. The bows measure about 31 inches long and have draw lengths of 26-30 inches. Hunting models were sold in camouflage patterns; target models were sold in gray, black, and wood-grain. The bows have laminated wood grips engraved with the word "BowTech" and a label with "The General" on the center pivot point of the bottom limb.

CPSCFeb 18, 2009Nationwide• BowTech Archery, of Eugene, Ore.

Abbott Laboratories: AxSYM System Tubing Decontamination Solution; 500 mL bott...

Bottle labels from lot 211974, AxSYM System Tubing Decontamination Solution (List Number 7B05-09), were found to be missing the following information: lot number, date of manufacture, and expiration date.

FDAFeb 18, 2009Nationwide• Abbott Laboratories