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Berko Electric, of Peru, Ind., now known as Marley Engineered Products, of Bennettsville, S.C.

Berko Electric, of Peru, Ind., now known as Marley Engineered Products, of Bennettsville, S.C. Recalls

All product recalls associated with Berko Electric, of Peru, Ind., now known as Marley Engineered Products, of Bennettsville, S.C..

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Recall Summary

Total Recalls

1000

Past Year

896

Class I (Serious)

125

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 15801–15820 of 17592 recalls

Toe-Space Electric Heaters (Berko Electric) – Fire Hazard (2007)

Fire/Burn Risk

The recall involves electric, toe-space heaters typically installed in kitchens and bathrooms at floor level in the recessed space under cabinets. The recall includes Berko Electric catalog numbers TS, TS-1 and TS-1A and Emerson Electric "Chromalox Comfort Heating" and "Environmental Products" catalog number KSH2000. The heater is controlled by a wall thermostat or a thermostat mounted on the front of the heater. The heater has a removable, black metal grille that measures 23 1/2 inches wide and 3 1/2 inches tall with five sets of openings, each with seven horizontal louvers.

CPSCAug 30, 2007Nationwide• Berko Electric, of Peru, Ind., now known as Marley Engineered Products, of Bennettsville, S.C.

Beckman Coulter Inc: Vidiera NsP Nucleic Sample Preparation, Part Number: A224...

Incorrect results: under certain circumstances, when transfer volume is not within the set range, the Vidiera NsP software does not report sample exclusion and does not flag the excluded sample in the "Run Results" report. The software error associated with the excluded sample appears as "Liquid was not successfully transferred to well#..........the sample will be excluded from further proce

FDAAug 30, 2007Nationwide• Beckman Coulter Inc

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Toshiba American Med Sys Inc: NEMIO XG Ultrasound System, Model SSA-580A , Software ver...

Multiple problems including : (1) The surface temperature of the transducer tip can rise and exceed the limit set by the international standard. (2) Incorrect display of the TI indices on the display monitor. The displayed value is greater or smaller than the true TI value, and (3) Manuals contain incorrect values for MI/TI values.

FDAAug 29, 2007Nationwide• Toshiba American Med Sys Inc

Toshiba American Med Sys Inc: NEMIO Ultrasound System, Model SSA-550A , Software versi...

FDAAug 29, 2007Nationwide• Toshiba American Med Sys Inc

Logger Boots (Wolverine) – Electrical Shock Risk (2007)

This recall involves Caterpillar brand steel toe logger boots. The boots were sold in women's and men's sizes. Women's boots were sold in black and have stock number P88030. Men's boots were sold in brown and black and have stock numbers P88033 or P88034. Stock numbers are printed on a label on the tongue of the shoe. The Caterpillar logo and "EH" are also printed on the label. The word "Caterpillar" is printed on the outside of the boots.

CPSCAug 28, 2007Nationwide• Wolverine World Wide Inc., of Rockford, Mich.

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Paceart System, 2006 Edition, Medtronic, Inc. 7...

An issue with the Paceart System - 2006 First Edition (Get Connected Edition) exists. Under certain circumstances, Paceart System Generic ICD reports may not accurately reflect patient VT/VF, SVT/NST and Mode Switch/AT/AF episode detection data. When episode detection data is imported into the Paceart System from certain sources, the Paceart System Generic ICD reports display a zero, suggesting

FDAAug 27, 2007Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Sofamor Danek USA Inc: Medtronic Sofamor Danek, TSRH SiLo 5.5 Spinal System, Sag...

Disassembly: The movable cradle component could detach from the saddle under extreme manipulation of the associated rods prior to final tightening of the set screws.

FDAAug 24, 2007Nationwide• Medtronic Sofamor Danek USA Inc

Backpack Blowers (Shindaiwa) – Fire Risk (2007)

Fire/Burn Risk

This recall involves Shindaiwa Models EB8510 and EB8510RT. All models up to serial #7025018 are included. After serial number 7025018, the leaf blower has been upgraded with stainless steel muffler shells. The backpack blowers weight approximately 24 pounds and include Serial Numbers through February 2007 production (S/N 702XXXX) which are located on the side label. These machines are blue, with a red label that reads "Shindaiwa".

CPSCAug 24, 2007Nationwide• Shindaiwa Kogyo Co., Ltd., Hiroshima, Japan

Philips Medical Systems North America Co. Phillips: Philips Medical System - BV Pulsera Mobile C-arms with Re...

System Shut Down -- Unexpected Shut Down during use of the Optional Remote Control.

FDAAug 23, 2007Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Philips Medical System - Endura X-Ray Systems (Release 2)...

System Shut Down -- Unexpected Shut Down during use of the Optional Remote Control.

FDAAug 23, 2007Nationwide• Philips Medical Systems North America Co. Phillips

Philips Nuclear Medicine, Inc.: The Pinnacle3 Radiation Therapy Planning (RTP) system and...

Incorrect Absolute Marking Coordinates when used with PQ-Series scanners due to a software malfunction

FDAAug 21, 2007AL, AK, AZ +43 more• Philips Nuclear Medicine, Inc.

Inotech Biosystems Intl., Inc: Inotech brand Heparin Adsorbant, Catalog #: HA-1, in 10m...

Erroneous Coagulation Tests

FDAAug 20, 2007Nationwide• Inotech Biosystems Intl., Inc

Beckman Coulter Inc: Cytomics FC 500 Flow Cytometry System with Data Innovatio...

Labeling provided by two integrated software systems are not clear enough to avoid potential demographic and sample type mismatches under certain conditions.

FDAAug 20, 2007Nationwide• Beckman Coulter Inc

Karl Storz Endoscopy America Inc 600 Corporate Pointe: Storz Equipment, Fluid Management Stand, for Fluid Manage...

Outflow Difference: The accuracy of the Equimat displayed value could be influenced by external factors of the cart/stand and may result in a fluctuating or inaccurate reading.

FDAAug 17, 2007Nationwide• Karl Storz Endoscopy America Inc 600 Corporate Pointe

Skil Circular Saws (Bosch) – Laceration Hazard (2007)

Laceration Risk

The recall involves Skil® brand circular saws with model numbers 5650, 5700, 5750 and 5755. The model number and date code are printed on the nameplate located on the front of the saw. The recall includes the following date codes: 28101 - 29231 38101 - 39231 48101 - 49231 58101 - 59231 68101 - 69231 No other models or date codes are included in this recall.

CPSCAug 15, 2007Nationwide• Robert Bosch Tool Corp., of Mount Prospect, Ill.

Classic Beauty Rest Electric Throws – Safety Issue (2007)

Fire/Burn Risk

This recall involves 52 inch by 62 inch electric warming throws. The 100% acrylic throws were sold in various colors and patterns and have model number BST-06-THR. The model number is located on the care label sewn into the throw. "Classic Beautyrest" and "Automatic Electric Warming Throw" is printed on the product's packaging. Model numbers with the following date codes are included in this recall: B00106 through B36506. Bilt-Safe Technologies, Inc. and the date code are printed on the bottom of the care label.

CPSCAug 15, 2007Nationwide• Ningbo Veken Elite International Trading Company Ltd., of China

Merit Medical Systems, Inc: Merit Medical Surgical Convenience Kits, Custom and SPPT,...

Expiration Dating; Some Convenience Kits contain medications and/or skin preparations that may expire before the expiration date on the outer package label.

FDAAug 15, 2007Nationwide• Merit Medical Systems, Inc

Smiths Medical MD, Inc.: Smiths Medical CADD-Sentry Pro Medication Safety Software...

Incorrect dosage possible: A software anomaly in the CADD-Sentry Pro Administrator software (version B) where the values of a weight based protocol go to zero or round up to the next higher hundredths place, even if Administrator displayed the values correctly at data entry.

FDAAug 14, 2007CO, MD, UT• Smiths Medical MD, Inc.

C.R. Bard Access Systems, Inc: Guidewire, 70cm x 1mm, REF 5583705, Sterile, Single Use, ...

Metal guidewires used in Hemodialysis Catheters may have been reverse loaded within the dispenser. Potential exists for the stiff end of the guidewire to be inserted into the patient instead of the flexible end.

FDAAug 10, 2007Nationwide• C.R. Bard Access Systems, Inc

Becton Dickinson & Company: Shelf Pack: Bard-Parker Rib-Back Carbon Steel no.11, surg...

Complaints received of rust on the blades of BD Bard-Parker Surgical blades.

FDAAug 10, 2007Nationwide• Becton Dickinson & Company