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Shenzhenshibangduoladianzikejimaoyi Co., Ltd. (Shenzhen Bangduola Electronic Technology Trade Co., Ltd.), of China

Shenzhenshibangduoladianzikejimaoyi Co., Ltd. (Shenzhen Bangduola Electronic Technology Trade Co., Ltd.), of China Recalls

All product recalls associated with Shenzhenshibangduoladianzikejimaoyi Co., Ltd. (Shenzhen Bangduola Electronic Technology Trade 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 1–20 of 398 recalls

Magnet Fidget Spinner Sets (Anzmtosn) – magnet ingestion (2025)

This recall involves Anzmtosn Magnet Fidget Spinner Sets. Each set contains 15 pieces and comes with four iridescent oval-shaped magnets, eight iridescent cuboidal-shaped magnetic stones, one red and yellow disk-shaped metal fidget spinner, one winged metal fidget spinner, and one multicolored infinity fidget cube. The set comes with a black fabric-lined storage case. The batch number, CCA06582, is printed on the back label of the packaging.

Very High

CPSCNov 20, 2025Nationwide• Shenzhenshibangduoladianzikejimaoyi Co., Ltd. (Shenzhen Bangduola Electronic Technology Trade Co., Ltd.), of China

Safe-T-Centesis 6 Fr Catheter Drainage Tray, REF: PIG1260T, (Bard Peripheral Vascular Inc 1625 W 3rd St Bldg 1 850 W. Rio Salado Prkwy. Tempe AZ 85281-2438) – laceration hazard (2025)

Laceration Risk

Acute drainage catheters, indicated for use in removing fluid during acute drainage/aspiration procedure, manufactured with safety indicators that erroneously show catheter in sharp position when catheter is in blunt position, which may lead users to believe device is not yet in pleural or peritoneal space when it is, may cause discomfort, delay to treatment, injury to internal organs or vessels.

Moderate

FDANov 6, 2025Nationwide• Bard Peripheral Vascular Inc 1625 W 3rd St Bldg 1 850 W. Rio Salado Prkwy. Tempe AZ 85281-2438

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Olympus OER-Pro (Aizu Olympus) – Maintenance Warning (2025)

Inform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance.

Low

FDAOct 31, 2025Nationwide• Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan

Olympus OER-Mini (Aizu Olympus) – Maintenance Warning (2025)

Inform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance.

Low

FDAOct 31, 2025Nationwide• Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan

Olympus OER-Elite (Aizu Olympus) – Maintenance Warning (2025)

Inform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance.

Low

FDAOct 31, 2025Nationwide• Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan

Pastured Grade AA Large Eggs (Kenz Henz) – Salmonella Contamination (2025)

Salmonella

Eggs may be contaminated with Salmonella.

Class IHigh

FDAOct 7, 2025TX• Kenz Henz LLC

Airvo 2 (Fisher & Paykel) – Power Disconnection Risk (2025)

When unintentionally disconnected from power source, humidifier device (used to deliver high flow warmed and humidified respiratory gases) may sound audible alert for less than 120 seconds, which may delay user awareness to reconnect power, which could lead to oxygen desaturation, hypoxia. Disinfection kit user manual updated to include checking the audible alert prior to use on a new patient.

Moderate

FDASep 18, 2025Nationwide• Fisher & Paykel Healthcare, Ltd. 15 Maurice Paykel Place East Tamaki Auckland New Zealand

Venclose digiRF Generator (Bard) – Wiring Detection Feature (2025)

Laceration Risk

Software version 3.35 of the Venclose digiRF Generator incorporates a catheter verification feature specifically designed to detect internal wiring anomalies in Venclose EVSRF Ablation Catheters prior to clinical use. This automated diagnostic check is executed immediately upon catheter connection to the generator, occurring before the procedure interface becomes accessible. When a catheter fails this verification process, the generator displays a Red X indicator on the screen without accompanying error codes, effectively disabling catheter functionality. However, BD has determined that software version 3.35 generates false positive failures due to temperature-dependent verification parameters, incorrectly flagging properly functioning Venclose EVSRF Ablation Catheters as defective when the catheter temperature is not at steady state during the check initiation.

High

FDAAug 21, 2025Nationwide• Bard Peripheral Vascular Inc 1625 W 3rd St Bldg 1 850 W. Rio Salado Prkwy. Tempe AZ 85281-2438

Kitchen Faucet (KICIMPRO) – Lead Exposure (2025)

This recall involves KICIMPRO kitchen faucets, model number KM800-01-06BN. The faucets are brushed nickel, single-handle kitchen faucets with a pull-down detachable spray and single-hole installation. Consumers can identify whether they have a recalled faucet by searching their Amazon purchase history for "Kicimpro" and "kitchen faucet" and looking for a description including pull-down sprayer, brushed nickel, high-arc, single-handle sink faucet with water lines, commercial modern RV stainless steel, grifos de cocina.

Very High

CPSCMay 29, 2025Nationwide• Kaipingshikemuyulinweiyushiyeyouxiangongsi, of China, doing business as Amazon seller Kicimpro

Gamma4 Right Long Nail (Stryker) – Incorrect Nail Geometry (2025)

Investigation confirmed that the GAMMA4 Right Long Nail was manufactured with the geometry of a left nail.

High

FDAMay 28, 2025Nationwide• Stryker GmbH Bohnackerweg 1 Selzach Switzerland

Femoral Nail T2 GTN (Stryker) – Incorrect Nail Version (2025)

Investigation determined that one lot of the T2 Greater Trochanter Nail (GTN) was labeled as left version but contained a right nail and another lot was labeled as right version but contained a left nail.

Moderate

FDAMay 22, 2025Nationwide• Stryker GmbH Bohnackerweg 1 Selzach Switzerland

Femoral Nail T2 GTN (Stryker) – Incorrect Nail Version (2025)

Moderate

FDAMay 22, 2025Nationwide• Stryker GmbH Bohnackerweg 1 Selzach Switzerland

Durango Gold (KZRV) – Step Assembly Mounting (2025)

K.Z., Inc. (KZRV) is recalling certain 2025 Durango Gold fifth wheels, equipped with a removable step assembly. The clip-on bracket mounting bolts may come loose, allowing the steps to detach.

High

NHTSAMay 6, 2025Nationwide• KZRV

Frozen Shrimp (Chicken of the Sea) – Undeclared Sulfites (2025)

Undeclared Allergen

Frozen Raw Peeled & Deveined tail on, shrimp contains undeclared sulfites

Class IHigh

FDAMay 6, 2025CO, IN• TRI-UNION FROZEN PRODUCTS INC DBA CHICKEN OF THE SEA FROZEN FOOD

Sample Probe (Beckman Coulter) – Manufacturing Defect (2025)

A manufacturing defect in the sample probe (S probe). The corners of the tip of the defective S probe are rounded and chamfered, which can prevent the proper formation of the "air layer" required for normal dispensing. The air layer is the air space that separates the cleaning water filled in the probe from the sample sucked into the probe. Maintaining this air space prevents the cleaning water and the sample from mixing. In the defective S probe, the "air layer" was not properly formed, causing the cleaning water and the sample to mix diluting the sample. As a result, the sample mixture dispensed into the cuvette has a lower concentration than the original sample, and the analyte concentration measured is lower than expected results.

Moderate

FDAApr 30, 2025Nationwide• Beckman Coulter Mishima K.K. 454-32 Higashino; Nagaizumi-Cho Sunto-Gun Japan

KliniTray Tissue Margin Board (Klinika Medical) – Microbial Contamination (2025)

Potential for microbial contamination.

Moderate

FDAApr 4, 2025Nationwide• Klinika Mdical Gmb Achtzehnmorgenweg 6 Usingen Germany

KliniTray Faxitron Plate (Klinika Medical) – Microbial Contamination (2025)

Potential for microbial contamination.

Low

FDAApr 4, 2025Nationwide• Klinika Mdical Gmb Achtzehnmorgenweg 6 Usingen Germany

Guide Wire with Ruler Tube (Stryker) – Metal Ring Detachment Risk (2025)

The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery.

Moderate

FDAMar 28, 2025Nationwide• Stryker GmbH Bohnackerweg 1 Selzach Switzerland

Guide Wire with Ruler Tube (Stryker) – Metal Ring Detachment Risk (2025)

The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery.

Moderate

FDAMar 28, 2025Nationwide• Stryker GmbH Bohnackerweg 1 Selzach Switzerland

Rotarex Atherectomy System (Bard) – catheter breakage (2025)

Atherectomy Catheter eIFU updated to clarify and emphasize procedural steps intended to reduce the likelihood of catheter breakage events. Catheter has an outer cylinder connected to a rotating helix, which could fracture and/or break, which would require retrieval, and helix facture/break could cause vessel injury and lead to severe bleeding.

High

FDAFeb 5, 2025Nationwide• Bard Peripheral Vascular Inc 1625 W 3rd St Bldg 1 850 W. Rio Salado Prkwy. Tempe AZ 85281-2438