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Shenzhen Haitan Technology Co. Ltd., d/b/a HTRC, of China

Shenzhen Haitan Technology Co. Ltd., d/b/a HTRC, of China Recalls

All product recalls associated with Shenzhen Haitan Technology Co. Ltd., d/b/a HTRC, of China.

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Recall Summary

Total Recalls

1000

Past Year

567

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 601–620 of 7756 recalls

C240 Battery Chargers (HTRC) - Fire Risk (2024)

Fire/Burn Risk

This recall involves HTRC C240 battery chargers sold for charging lithium-ion batteries. The defective chargers are black with two blue screens, numbered 1 and 2, and the model identifier "C240 DUO" printed between the screens. The brand name "HTRC" is printed at the bottom left corner.

CPSCDec 12, 2024Nationwide• Shenzhen Haitan Technology Co. Ltd., d/b/a HTRC, of China

Dabigatran Etexilate 75mg (Ascend) – Impurity Limit Exceeded (2024)

CGMP Deviations: Presence of N-nitroso-Dabigatran impurity above recommended interim limit

Class IIModerate

FDADec 12, 2024Nationwide• Ascend Laboratories, LLC

Dabigatran Etexilate 150mg (Ascend) – Impurity Limit Exceeded (2024)

CGMP Deviations: Presence of N-nitroso-Dabigatran impurity above recommended interim limit

1...29 303132 33...388

Page 31 of 388Next

Class IIModerate

FDADec 12, 2024Nationwide• Ascend Laboratories, LLC

ACCOLADE DR Pacemaker (Boston Scientific) – Safety Mode Potential (2024)

A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built before September 2018, have an increased potential to initiate Safety Mode during telemetry or other normal, higher-power operations due to latent high battery impedance.

FDADec 12, 2024Nationwide• Boston Scientific Corporation

Idylla Instrument (Biocartis) – False-Positive MSI-H Results (2024)

False-positive MSI-H results generated by the Idylla MSI Test.

FDADec 10, 2024AL, CA, NJ +2 more• Biocartis Nv B 3 Generaal De Wittelaan 11 Mechelen Belgium

Duloxetine Capsules 30mg (Breckenridge) – CGMP Impurity Limit (2024)

CGMP Deviations: presence of N-nitroso-duloxetine impurity above FDA recommended interim limit.

Class IIModerate

FDADec 6, 2024Nationwide• Breckenridge Pharmaceutical, Inc

Duloxetine Capsules 60mg (Breckenridge) – CGMP Impurity Limit (2024)

CGMP Deviations: presence of N-nitroso-duloxetine impurity above FDA recommended interim limit.

Class IIModerate

FDADec 6, 2024Nationwide• Breckenridge Pharmaceutical, Inc

Cascade Raw Cheddar (Heber Valley) – E. coli risk (2024)

E. coli

The Cascade Raw Cheddar Cheese was recalled due to Shiga toxin-producing E. coli (STEC) and elevated generic E.coli in finished product testing results.

Class IHigh

FDADec 6, 2024MT, NV, UT +1 more• Heber Valley Artisan Cheese, LLC.

Ultrasoft Oxygen Cannula (3B Medical) – Expired Product (2024)

The devices were inadvertently shipped after their expiration date.

FDANov 27, 2024AR, MA• 3B Medical, Inc. 203 Avenue A Nw Ste 300 Winter Haven FL 33881-4540

Access Intact PTH Assay (Beckman Coulter) – Reagent Dispense Issue (2024)

Beckman Coulter has identified that some Access PTH reagent packs from lot 339071 may be over- or under-filled in well 0. The dispensed material in well 0 could be above or below specification, risking sealing issues, contamination, instrument errors, delays, or inaccurate results with a negative bias and increase in imprecision. The issue was confirmed on 10 April 2024 by Beckman Coulter through an internal non-conformance (NC-INT-66585). The well 0 scale on the filling line began malfunctioning on the fill immediately before PTH. The malfunction was not noticed until the majority of PTH was filled.

FDANov 26, 2024Nationwide• Beckman Coulter, Inc.

Xhibit Telemetry Receiver (Spacelabs) – Windows Proxy Issue (2024)

Telemetry receiver systems may experience a Windows proxy Issue causing the system to shut down and restart (Offline displayed), lasting approximately 1 to 1.5 minutes, which will cause temporary loss of monitoring. If a clinical event occurred during this period, staff may not detect until the system restarts; necessary clinical intervention could be delayed.

FDANov 25, 2024AL, AK, AZ +41 more• Spacelabs Healthcare, Inc.

Eclipse PRO Holter Recorder (Spacelabs) – Serial Number Error (2024)

Due to a manufacturing error the incorrect device serial number was potentially programmed into the holter recorder. The physical serial number label on the device might not match the serial number programmed into the device.

FDANov 25, 2024AR, CA, CO +19 more• Spacelabs Healthcare, Ltd. Unit B Foxholes Centre; John Tate Road Hertford United Kingdom

Crab Cheese Rangoon (Tampa Food) – Undeclared Allergens (2024)

Undeclared Allergen

Undeclared allergens: Milk, Soy, Crustacea Shellfish, Fish

Class IHigh

FDANov 25, 2024FL• SE Tampa Inc dba Tampa Food

Eclipse Mini Holter Recorder (Spacelabs) – Serial Number Error (2024)

FDANov 25, 2024AR, CA, CO +19 more• Spacelabs Healthcare, Ltd. Unit B Foxholes Centre; John Tate Road Hertford United Kingdom

Xhibit Telemetry Receiver (Spacelabs) – System Shutdown Risk (2024)

Telemetry receivers with affected software versions may experience unsolicited system shut down and restart (Offline displayed), lasting approximately 1 to 1.5 minutes, which will cause temporary loss of monitoring. If a clinical event occurred during this period, staff may not detect until the system restarts and necessary clinical intervention could be delayed.

FDANov 25, 2024AL, AR, CO +24 more• Spacelabs Healthcare, Inc.

Javygtor Tablets 100mg (Dr. Reddy's) – Impurity Specifications (2024)

Failed Impurities/Degradation Specifications

Class IIILow

FDANov 22, 2024Nationwide• Dr. Reddy's Laboratories, Inc.

Technetium Tc 99m Sulfur Colloid Kit (Jubilant Radiopharma) – Stability Failure (2024)

Failed Stability Specifications

Class IIModerate

FDANov 22, 2024Nationwide• Jubilant Draximage Inc., dba Jubilant Radiopharma

StatStrip Glucose Ketone Meter (Nova Biomedical) – Result Error (2024)

A software bug within the meter firmware leads to transmission of erroneous glucose and/or ketone patient test results to a healthcare institution's data management system (DMS) at healthcare sites using WiFi if a user navigates to the Review Results screen while the meter is in the process of transmitting the current test result to the DMS.

FDANov 20, 2024Nationwide• Nova Biomedical Corporation

StatStrip Glucose Ketone Meter (Nova Biomedical) – Result Error (2024)

FDANov 20, 2024Nationwide• Nova Biomedical Corporation

StatStrip Glucose Meter (Nova Biomedical) – Result Transmission Error (2024)

A software bug within the Gen 2 StatStrip Hospital Meter firmware leads to transmission of erroneous glucose patient test results to a healthcare institution's data management system (DMS) at healthcare sites using WiFi if a user navigates to the Review Results screen while the meter is in the process of transmitting the current glucose test result to the DMS. The risk of this software defect is erroneously high or low glucose results being documented in a patient's medical record, which may lead to incorrect treatment.

FDANov 20, 2024Nationwide• Nova Biomedical Corporation