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Shaoxingkeqiao Nenghaozhenfang Co. Ltd., of China

Shaoxingkeqiao Nenghaozhenfang Co. Ltd., of China Recalls

All product recalls associated with Shaoxingkeqiao Nenghaozhenfang Co. Ltd., of China.

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Recall Summary

Total Recalls

398

Past Year

Class I (Serious)

Most Recent

Nov 2025

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 21–40 of 398 recalls

Roller Window Shades (ChrisDowa) – Strangulation Risk (2025)

This recall involves ChrisDowa Roller Window Shades sold exclusively on Amazon.com. The roller blinds were sold in multiple colors, with sizes ranging from a width of 20-27 inches and height of 72 inches. ChrisDowa is printed on the label sticker on the headrail.

High

CPSCJan 23, 2025Nationwide• Shaoxingkeqiao Nenghaozhenfang Co. Ltd., of China

DxC 500 AU Analyzer (Beckman) – Stability Date Issue (2025)

Beckman Coulter has identified an issue which prevents the DxC 500 AU instrument from providing the correct onboard stability (Open Expiration) dates for assays that were loaded prior to a software upgrade (e.g. 1.3 to 1.4, 1.4 to 1.4.1, etc.). As a result, assays that have expired may still be used for sample processing, leading to inaccurate or erroneous patient test results. The issue only happens on assays loaded before instruments doing upgrades and does not impact new installation. It does not impact the assays loaded after upgrade.

High

FDAJan 10, 2025AL, CA, CO +16 more• BECKMAN COULTER LABORATORY SYSTEMS (SUZHOU) CO., LTD. No.

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KARL STORZ Uretero-Renoscope (Karl Storz) – Reprocessing Modality Issue (2024)

Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.

Moderate

FDADec 19, 2024Nationwide• Karl Storz Endoscopy

Karl Storz Endoskope Biopsy Forceps (Karl Storz) – Cleaning Validation Failure (2024)

Due to failure of manual cleaning validation, biopsy and grasping forceps like sterility assurance.

Moderate

FDADec 19, 2024AZ, AR, CA +29 more• Karl Storz Endoscopy

KARL STORZ Uretero-Renoscope (Karl Storz) – Reprocessing Modality Issue (2024)

Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.

Moderate

FDADec 19, 2024Nationwide• Karl Storz Endoscopy

KARL STORZ Uretero-Renoscope (Karl Storz) – Reprocessing Modality Issue (2024)

Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.

Moderate

FDADec 19, 2024Nationwide• Karl Storz Endoscopy

KARL STORZ Cysto-Urethroscope (Karl Storz) – Reprocessing Modality Issue (2024)

Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.

Moderate

FDADec 19, 2024Nationwide• Karl Storz Endoscopy

KARL STORZ Uretero-Renoscope (Karl Storz) – Reprocessing Modality Issue (2024)

Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.

Moderate

FDADec 19, 2024Nationwide• Karl Storz Endoscopy

KARL STORZ Pediatric Uretero-Renoscope (Karl Storz) – Reprocessing Issue (2024)

Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.

Moderate

FDADec 19, 2024Nationwide• Karl Storz Endoscopy

KARL STORZ Uretero-Renoscope (Karl Storz) – Reprocessing Modality Issue (2024)

Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.

Moderate

FDADec 19, 2024Nationwide• Karl Storz Endoscopy

Otological Ventilation Tube (Adept Medical) – Clearance Issue (2024)

Lack of 510(k) clearance.

Low

FDANov 24, 2024Nationwide• Adept Medical Ltd 2-6 Mc Donald Street Morningside, Po Box 10075 Dominion Rd Auckland New Zealand

2025 KZRV Sportsmen (KZRV) – door slide-out actuator risk (2024)

KZRV, L.P (KZRV) is recalling certain 2025 Sportsmen 303QBSE travel trailers. The driver's side door slide-out actuator is located too close to the tires, which can cause the actuator to contact the tire.

High

NHTSANov 1, 2024Nationwide• KZRV

Karl Storz Irrigation Tubing (Karl Storz) – Labeling Error (2024)

Due to improper labeling of products. An intended use on the label has not been reviewed and approved by FDA for distribution in the U.S.

Low

FDAOct 21, 2024Nationwide• Karl Storz Endoscopy

Karl Storz Aggressive Cutter (Karl Storz) – Sterility Barrier Breach (2024)

Due to holes detected in the inner barrier system that may compromise the sterility of the affected products.

High

FDAOct 11, 2024Nationwide• Karl Storz Endoscopy

Bard Marquee Biopsy Instrument Kit (Bard) – Needle Retention Defect (2024)

Disposable biopsy instruments were potentially manufactured missing the backend notch retention feature on the needle that results in inadequate securing of the needle inside the device, which could lead to needle detachment and misplacement, which could lead to tissue damage and bleeding.

Moderate

FDASep 30, 2024Nationwide• Bard Peripheral Vascular Inc 1625 W 3rd St Bldg 1 850 W. Rio Salado Prkwy. Tempe AZ 85281-2438

EVSRF Catheter (Bard) – Wiring Error Risk (2024)

The Venclose" RF Ablation Catheters may have been manufactured with internal wiring error. The red and yellow signal wires were soldered on swapped ports of the catheter PCB. This error in wire configuration would lead to power being applied through the proximal 3/4th of the heating coil, bypassing the thermocouple, which will then cause the generator to overdrive the catheter in an attempt to reach desired temperature set point. The wire attachment error causes the device to reach temperatures exceeding the levels intended for therapeutic efficacy, while the console is falsely indicating that temperature has not yet been reached, thus increasing the risk of harm due to excessive temperature.

High

FDASep 4, 2024Nationwide• Bard Peripheral Vascular Inc 1625 W 3rd St Bldg 1 850 W. Rio Salado Prkwy. Tempe AZ 85281-2438

Airvo 3 Respiratory Device (Fisher & Paykel) - High Pressure Oxygen Risk (2024)

Due to a software issue, affected devices that are set up with High Pressure Oxygen (HPO), if the flow alignment alarm occurs, the device will deliver room air only. If this happens, a patient my experience oxygen desaturation that could lead to hypoxia.

High

FDAAug 7, 2024AZ, CA, CO +26 more• Fisher & Paykel Healthcare, Ltd. 15 Maurice Paykel Place East Tamaki Auckland New Zealand

BARD MAGNUM Biopsy Needle (Bard) – Packaging Damage (2024)

Laceration Risk

Due to possible packaging damage (indentations/cuts) cause by manufacturing process. As a result of the packaging damage, may cause the sterile barrier to be compromised.

Moderate

FDAAug 2, 2024Nationwide• Bard Peripheral Vascular Inc 1625 W 3rd St Bldg 1 850 W. Rio Salado Prkwy. Tempe AZ 85281-2438

ECHO Gas-Powered Backpack Blowers (ECHO) – fire hazard (2024)

Fire/Burn Risk

This recall involves two ECHO 59.7cc gas-powered backpack blowers with the model numbers PB-5810H and PB-5810T. These blowers are designed for residential and commercial use. The blowers are orange and black in color, and "ECHO" is printed on the starter recoil housing. Model and serial numbers are located on a label near the right side of the black blower fan housing. This recall includes the following serial numbers: Model Number Serial Number Range PB-5810H P61312001001 to P61312002590 PB-5810T P61212001001 to P61212004155

High

CPSCAug 1, 2024Nationwide• ECHO Inc., of Lake Zurich, Illinois

Karl Storz - Endoskope , REF: 27294AA, Hopkins Telescope ... (Karl Storz Endoscopy) – various medical device product ifus c... (2024)

Various medical device product IFUs contain reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.

Moderate

FDAJul 23, 2024Nationwide• Karl Storz Endoscopy