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Carbon Medical Technologies, Inc.

Carbon Medical Technologies, Inc. Recalls

All product recalls associated with Carbon Medical Technologies, Inc..

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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 1941–1960 of 21320 recalls

BiomarC EX Fiducial Marker System, Catalog Number 040165 (Carbon Medical Technologies, Inc.) – this recall has been initiated due to... (2024)

This recall has been initiated due to a failure to provide an MRI Insert that is to be provided to the patient.

Low

FDAJul 26, 2024Nationwide• Carbon Medical Technologies, Inc.

ADVIA Centaur CA 19-9 (250 Test)-In vitro diagnostic use ... (Siemens Healthcare Diagnostics, Inc.) – positive bias for some samples around... (2024)

Positive bias for some samples around the CA 19-9 upper limit of normal of 35 U/m as compared to the previous lot. The sample bias observed was greatest in the Asia Pacific sample population. The observed bias is not proportional across the assay measuring interval and is less pronounced for sample results above a concentration of 110 U/mL.

Moderate

FDAJul 26, 2024Nationwide• Siemens Healthcare Diagnostics, Inc.

Atellica IM CA 19-9 (Siemens) – Test Result Bias (2024)

1...96 979899 100...1066

Page 98 of 1066Next

Moderate

FDAJul 26, 2024Nationwide• Siemens Healthcare Diagnostics, Inc.

Atellica IM CA 19-9 (250 Test - REF)-In vitro diagnostic ... (Siemens Healthcare Diagnostics, Inc.) – positive bias for some samples around... (2024)

Moderate

FDAJul 26, 2024Nationwide• Siemens Healthcare Diagnostics, Inc.

ADVIA Centaur CA 19-9 (50 Test)-In vitro diagnostic use i... (Siemens Healthcare Diagnostics, Inc.) – positive bias for some samples around... (2024)

Moderate

FDAJul 26, 2024Nationwide• Siemens Healthcare Diagnostics, Inc.

Mountain 600 Snowmobiles (Arctic Cat) – crash hazard (2024)

This recall involves 2024 Arctic Cat Mountain 600 Snowmobiles, sold in various colors. The model name is depicted as an "M" in the shape of a mountain and is printed on the side panels of the snowmobiles. The 10th digit of the VIN is "R". The VIN number is stamped on the tunnel section or the decal on the top/rear of the tunnel.

High

CPSCJul 25, 2024Nationwide• Textron Specialized Vehicles, of Augusta, Georgia

Wood Dining Chairs (Grand Rapids) – Fall Hazard (2024)

This recall involves Brooke model chairs including: all wood dining chairs in several styles, including partially and fully upholstered seats, and fully upholstered seat and back. The model numbers W520, W520-11, W520-21, W520-31, and W520-33 can be found on the original order confirmation or invoice. If not available, reference the Special Order Number ("SO#") found on the white sticker on the underside of each chair. A list of affected special order numbers can be found at www.grandrapidschair.com/customer-service/product-safety-recall-brooke/.

Moderate

CPSCJul 25, 2024Nationwide• Grand Rapids Chair Company, of Byron Center, Michigan

Barricaid Annular Closure Impactor, REF: BAR-IMPACTOR, P/... (Intrinsic Therapeutics, Inc.) – at least two units have been found to... (2024)

At least two units have been found to be missing a weld.

High

FDAJul 25, 2024Nationwide• Intrinsic Therapeutics, Inc.

Vivo 45 LS, pressure and volume ventilator capable of del... (Breas Medical, Inc.) – there is a potential for short term (... (2024)

There is a potential for short term (<7 days) elevated levels of formaldehyde emitted from the device into the patient breathing airpath in specific conditions.

Moderate

FDAJul 25, 2024Nationwide• Breas Medical, Inc.

NEUROSIGN Disposable Stimulating Dissector, REF 5888-00 (Technomed Europe Amerikalaan 71 Maastricht-Airport Netherlands) – product has have presence of brown di... (2024)

Product has have presence of brown discoloration or substance on the hinge area of the device

Low

FDAJul 25, 2024CA, FL, IL +4 more• Technomed Europe Amerikalaan 71 Maastricht-Airport Netherlands

McKesson Syringe 60CC, Luer Lock Tip, Sterile, ITEM NO 10... (Cypress Medical Products LLC) – affected syringes lack fda clearance (2024)

Affected syringes lack FDA clearance.

High

FDAJul 24, 2024Nationwide• Cypress Medical Products LLC

Sodium Chloride Injection (B. Braun) – Particulate Matter (2024)

Presence of Particulate Matter

Class IHigh

FDAJul 24, 2024Nationwide• B. Braun Medical Inc

VariSoft Infusion Set, Single Use. (Unomedical A/S Osted Aholmvej 1) – specific varisofttm infusion sets wer... (2024)

Specific VariSoftTM Infusion Sets were packaged using incorrect secondary packaging (boxes) branded "Trusteel Infusion Set".

Low

FDAJul 23, 2024Nationwide• Unomedical A/S Osted Aholmvej 1

Desflurane E_Vap.(Saf-T-Fill) used with the A9 Anesthesia... (Mindray DS USA, Inc. dba Mindray North America) – v90 electronic vaporizer anesthetic a... (2024)

V90 electronic vaporizer anesthetic agent output may be higher than the set amount due to a component within the vaporizer causing an incomplete seal in some cases. Should this issue occur, the A9 Anesthesia System will generate alarms associated with abnormal vaporizer output. If the anesthetic concentration is too high, the patient can inhale too much anesthetic agent; the patient may suffer from symptoms such as vertigo and drowsiness after the operation. In severe cases, the patient may suffer from neurological sequelae such as hypomnesia and inattention

Moderate

FDAJul 22, 2024CA, GA, KY +6 more• Mindray DS USA, Inc. dba Mindray North America

SlideView VS200 slide viewer, (EVIDENT SCIENTIFIC INC) – a broken fuse inside the laser that w... (2024)

A broken fuse inside the laser that was caused by a short circuit at PIN 4 of the DOOR CTRL. This short circuit was caused by a badly positioned cable that made contact with the housing/frame and caused a short circuit and destroyed the fuse in the laser. This caused the shutter to remain in its most recent state; either in an open or closed position. Once the fuse was destroyed the shutter could not be operated.

Moderate

FDAJul 22, 2024Nationwide• EVIDENT SCIENTIFIC INC

Isoflurane E_Vap.(Safety Filling adapter): used with the ... (Mindray DS USA, Inc. dba Mindray North America) – v90 electronic vaporizer anesthetic a... (2024)

Moderate

FDAJul 22, 2024CA, GA, KY +6 more• Mindray DS USA, Inc. dba Mindray North America

Azelaic Acid Gel (Glenmark) – CGMP Deviation (2024)

CGMP Deviations

Class IIModerate

FDAJul 22, 2024Nationwide• Glenmark Pharmaceuticals Inc., USA

Sevoflurane E_Vap.(Quik-Fil):used with the A9 Anesthesia ... (Mindray DS USA, Inc. dba Mindray North America) – v90 electronic vaporizer anesthetic a... (2024)

Moderate

FDAJul 22, 2024CA, GA, KY +6 more• Mindray DS USA, Inc. dba Mindray North America

Sevoflurane E_Vap.(Safety Filling adapter) used with the ... (Mindray DS USA, Inc. dba Mindray North America) – v90 electronic vaporizer anesthetic a... (2024)

Moderate

FDAJul 22, 2024CA, GA, KY +6 more• Mindray DS USA, Inc. dba Mindray North America

Apple Danish (SSP America) – Incorrect ingredient label (2024)

Allergens were declared but the finished product label incorrectly listed ingredients of Almond Croissant.

Class IIModerate

FDAJul 19, 2024AZ• SSP America PHX, LLC