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Shanghai MeiHao Electric Co. Ltd., of Shanghai, China

Shanghai MeiHao Electric Co. Ltd., of Shanghai, China Recalls

All product recalls associated with Shanghai MeiHao Electric Co. Ltd., of Shanghai, China.

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Recall Summary

Total Recalls

1000

Past Year

631

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 10061–10080 of 10391 recalls

BLACK CAT Electric Pressure Washer – Safety Hazard (2004)

The recalled pressure washers have a black plastic housing and a BLACK CAT® logo on both sides of the unit. "MCM International," "Model TW1800" or "Model BC2200" appear on a silver label on the recalled units.

CPSCNov 15, 2004Nationwide• Shanghai MeiHao Electric Co. Ltd., of Shanghai, China

Baxter Healthcare Renal Div: Baxter CAPD Solution Transfer Set for use with UV-Flash G...

Disconnection of the tubing at the clamp level of the UV Flash Transfer Set.

FDANov 5, 2004Nationwide• Baxter Healthcare Renal Div

Baxter Healthcare Corp. Rt.: Colleague 3 CX Triple Channel Volumetric Infusion Pumps, ...

A software anomaly causes a failure alarm code 12:303 which audibly alarms and stops the function of all channels in use. This causes an interruption in therapy, which may result in a risk to the patient.

1...502 503504505 506...520

Page 504 of 520Next

FDANov 4, 2004Nationwide• Baxter Healthcare Corp. Rt.

Brake Parts Cleaner (Valvoline) – Chemical Risk (2004)

The recall involves 13-ounce cans of Pyroil® Non-Chlorinated Brake Parts Cleaner and NAPA® Non-Chlorinated Brake Cleaner. This product is used by professional mechanics as well as "do-it-yourself" consumers who perform brake repairs on their own vehicles. The recalled cans contain one of the following four digits in their date codes, which are found on the bottom of the cans: Pyroil (Part No. 4003) C014 C024 C184 C194 C304 D024 D034 D214 D224 D264 E104 F074 F084 F094 F104 F234 F244 F284 G134 G144 G194 G294 H034 H194 NAPA (Part No. 4800) C024 C094 C184 C194 C224 C234 C304 C314 D014 D034 D054 E054 E064 E144 E244 E254 F174 F184 G284 H124 H304 H314 I074 I084

CPSCNov 4, 2004Nationwide• The Valvoline Company, a Division of Ashland Inc., of Lexington, Ky.

Baxter Healthcare Corp. Rt.: Colleague Single Channel Volumetric Infusion Pumps, produ...

FDANov 4, 2004Nationwide• Baxter Healthcare Corp. Rt.

Hampton Bay Halogen Light Fixture – Safety Issue (2004)

Fire/Burn Risk

The recall involves the Hampton Bay® three-head, flush-mount, halogen light fixture with silver metal rings on the lamp fixtures. It is 15.75 inches wide by 6 inches high. The lights have frosted glass shades. The position of the three lamps on the fixture can be adjusted by turning and bending the lamp heads. A clear label on the fixture reads "MADE IN CHINA," and "E91785."

CPSCNov 4, 2004Nationwide• Cordelia Lighting, of Rancho Dominguez, Calif.

Baxter Healthcare Corp. Rt.: Colleague 3 Triple Channel Volumetric Infusion Pumps, pro...

FDANov 4, 2004Nationwide• Baxter Healthcare Corp. Rt.

Baxter Healthcare Corp. Rt.: Colleague CX Single Channel Volumetric Infusion Pumps, pr...

FDANov 4, 2004Nationwide• Baxter Healthcare Corp. Rt.

Arc Fault Circuit Interrupters (Schneider) – Electrical Defect (2004)

Fire/Burn Risk

The recalled Square D QO® and Homeline® Arc Fault Interrupter circuit breakers are used with 15- and 20-amp branch circuits. They are required to be installed in bedroom circuits in accordance with the 2002 National Electrical Code. The recalled units were manufactured after March 1, 2004, and have a blue test button. The AFCI circuit breakers have one of the following date codes - CN, DN, EN, FN, GN, HN, or JN - stamped in red on the breaker label located just above the wiring terminal. The recalled units also have one of the following catalog numbers printed on a label on the front of the breaker: QO115AFI, QO115AFIC, QO120AFI, QO120AFIC, QOB115AFI, QOB120AFI, HOM115AFI, HOM115AFIC, HOM120AFI, HOM120AFIC, QO115VHAFI, QO120VHAFI, QOB115VHAFI, or QOB120VHAFI.

CPSCNov 3, 2004Nationwide• Schneider Electric North American Division, of Palatine, Ill.

Harvard Clinical Technology: Harvard 2 Dual Channel Syringe Infusion Pump P/N 2001-001

Potential pump motor/encoder assembly failure may cause over infusing medication in patients

FDANov 3, 2004AK, CA, CT +18 more• Harvard Clinical Technology

Harvard Clinical Technology: Harvard 1 Single Channel Syringe Infusion Pump, P/N 2003-001

Potential pump motor/encoder assembly failure may cause over infusing medication in patients

FDANov 3, 2004AK, CA, CT +18 more• Harvard Clinical Technology

Harvard Clinical Technology: Harvard 2 Syringe Pump manufactured for Rita Medical (OEM...

Potential pump motor/encoder assembly failure may cause over infusing medication in patients

FDANov 3, 2004AK, CA, CT +18 more• Harvard Clinical Technology

Omron Healthcare, Inc.: Medication Bottle (U22-3), a component of the MicroAir Vi...

A potential failure of the vibrating mechanism of the medication bottle which causes a failure to transmit vibration and results in no nebulization.

FDANov 2, 2004Nationwide• Omron Healthcare, Inc.

Baxter Healthcare Renal Div: HomeChoice and Yume Automated Peritoneal Dialysis Systems...

The on/off power switch is not grounded as a separate component in the device, and can loosen from its housing, which may result in an electrical shock to the user.

FDANov 1, 2004Nationwide• Baxter Healthcare Renal Div

Robertshaw TS-11 Gas Valve (Robertshaw) – Commercial Equipment Risk (2004)

Fire/Burn Risk

The TS-11 Thermal Safety Control Gas Valves are installed in commercial cooking equipment with pilot lights, including ranges, griddles, fryers, and warming trays. The recalled gas valves were produced between February 2003 and August 2004. The "magnet heads" on the gas valves were made during the same range of dates. The recalled products can be identified by date codes 0306 through and including 0432. The TS-11 gas valve with different manufacturing dates and a different hazard was recalled in 2002.

CPSCNov 1, 2004Nationwide• Robertshaw Controls Company of Long Beach, California

Baxter Healthcare Renal Div: HomeChoice PRO and Yume Plus Automated Peritoneal Dialysi...

The on/off power switch is not grounded as a separate component in the device, and can loosen from its housing, which may result in an electrical shock to the user.

FDANov 1, 2004Nationwide• Baxter Healthcare Renal Div

Cardinal Health 1430 Waukegan Rd Attn V. Mueller Qa McGaw Park IL 60085: V. Mueller Pfister-Schwartz Stone Retriever 4-Wire Basket...

The dispenser box was mislabeled with the wrong length and the wrong wire gauge.

FDAOct 27, 2004MS, MO, NY +4 more• Cardinal Health 1430 Waukegan Rd Attn V. Mueller Qa McGaw Park IL 60085

Abbott Health Products, Inc.: IMx HAVAB Controls are for In Vitro Diagnostic use. The k...

Abbott identified through investigational studies that IMx HAVAB Controls lot 18220Q100 is generating Negative Control values outside the upper range specified in the IMx HAVAB Package Insert.

FDAOct 27, 2004AZ, CA, IL +10 more• Abbott Health Products, Inc.

Mainstays Garden Folding Lawn Chair (Rio Brands) – Structural Failure (2004)

The recalled folding lawn chairs have green plastic arms with green steel folding frames or blue plastic arms with blue folding steel frames. They are constructed of matching vinyl webbing. The chairs measure 31 inches high and 22.5 inches wide. The left-hand arm of the chairs has the word "RIO" on it. Only the chairs with green or blue plastic arms are included in this recall.

CPSCOct 26, 2004Nationwide• Rio Brands, of Philadelphia, Pa.

Medtronic Inc. Cardiac Rhythm Managment: Medtronic CapSureFix Novus Lead Model 5076.

A specific lot of leads are labeled incorrectly. The leads are 45 cm in length and labeled as 52 cm lead length.

FDAOct 20, 2004Nationwide• Medtronic Inc. Cardiac Rhythm Managment