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Briggs & Stratton Power Products Group, LLC, of Milwaukee, Wis.

Briggs & Stratton Power Products Group, LLC, of Milwaukee, Wis. Recalls

All product recalls associated with Briggs & Stratton Power Products Group, LLC, of Milwaukee, Wis..

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Recall Summary

Total Recalls

1000

Past Year

888

Class I (Serious)

124

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 12421–12440 of 17593 recalls

Rear Engine Riding Mower (Briggs & Stratton) – Injury Risk (2014)

This recall involves six models of Briggs and Stratton Snapper Rear Engine Riding Mowers. The mowers are red with a black fuel tank, steering wheel and seat. The name Snapper is printed on both sides of the mower. The model and serial numbers are on a label on the engine platform under the right side of the seat. The following models and serial number ranges are included. Model Number Serial Number Range 7800918 2016447188 - 2016485206 7800920 2016443919 - 2016568930 7800932 2016462619 - 2016481454 7800950 2016611952 - 2016766052 7800951 2016624456 - 2016765000 7800954 2016603229 - 2016775752

CPSCOct 16, 2014Nationwide• Briggs & Stratton Power Products Group, LLC, of Milwaukee, Wis.

AMS Monarc Subfascial Hammock (AMS) - Packaging Concern (2014)

During routine periodic packaging testing, AMS identified that in simulated extreme shipping and handling situations the sterile barrier packaging of the Needle Passer components supplied with the AdVance" Male Sling System; Model # 720088-01; AdVance" XP Male Sling System; Model # 720163-01; Monarc" C Subfacial Hammock; Model # 72404195; Monarc" + Subfacial Hammock; Model #

Class IIModerate

FDAOct 15, 2014Nationwide• American Medical Systems, Inc.

1...620 621622623 624...880

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AdVance Male Sling System (AMS) - Packaging Concern (2014)

Class IIModerate

FDAOct 15, 2014Nationwide• American Medical Systems, Inc.

Dutchmen Rubicon (Dutchmen) - Fuel System Issue (2014)

Fire/Burn Risk

Keystone RV Company (Keystone) is recalling certain model year 2015 Dutchmen Rubicon trailers manufactured August 22, 2014, to September 17, 2014. The affected vehicles may have been assembled with the clamp installed incorrectly on the fuel line at the generator fuel filter and the fuel tank. As a result, the fuel line may disconnect.

NHTSAOct 10, 2014Nationwide• DUTCHMEN

AMS 700 Series Penile Prosthesis (AMS) - Needle Recall (2014)

AMS' supplier has issued a recall of certain lots of Lightning Bolt Keith needles supplied in AMS 700 Accessory Kits. Based on this, AMS is recalling AMS 700 Accessory Kits which contain these lots of needles. The supplier made the decision to issue this recall after an internal investigation that was requested by AMS. The investigation identified a potential nonconformity that may lead to a bent or broken Keith Needle when used with the Furlow tool.

Class IIModerate

FDAOct 10, 2014Nationwide• American Medical Systems, Inc.

Gel-E Donut (Philips) - Mold Contamination (2014)

Mold on gel filled Gel-E and Squishon products

Class IHigh

FDAOct 10, 2014Nationwide• Philips Medical Systems, Inc.

Medstream Administration Sets (US Infusion) - Leakage Problem (2014)

Several complaints regarding the IV sets leaking at the Y site.

Class IIModerate

FDAOct 10, 2014CA, GA, IL +4 more• US Infusion Inc dba Trucare Biomedix-USA

TITAN Operating Room Table (Trumpf) - Unintended Movement (2014)

Unintended movement of the operating table during surgical cases due to the use of damaged TITAN remotes.

Class IIModerate

FDAOct 9, 2014Nationwide• Trumpf Medical Systems, Inc.

Haleigh Wire Dome Pendant (Rejuvenation) – Injury potential (2014)

This recall involves Rejuvenation Haleigh Wire Dome Pendant hanging lamps sold in three different finishes: Lacquered polished brass, oil rubbed bronze and polished nickel. The lamp is a parabolic-shaped dome made of solid brass with an external wire structure and a ceiling plate. The lamp cord can vary in length from 14 inches to 200 inches. The lamps are illuminated by one 150-watt bulb. The lamp's canopy measures 5 ¼ inches wide and 12 inches long for item # A5908 or 8 inches long for item # A5909. The item number can be found on a white label inside the ceiling plate.

CPSCOct 9, 2014Nationwide• Rejuvenation Inc., of Portland, Ore., a division of Williams-Sonoma

Low Water Cut-Off Control Units (Fluid Handling) – Fire hazard (2014)

Fire/Burn Risk

This recall involves McDonnell and Miller series 750 Low Water Cut-Off control units, which in connection with a water level sensor, are used as a primary or secondary safety control on hot water or steam boilers to signal the boiler to provide protection in low water conditions. The unit is mounted on the outside of a boiler, generally near the boiler's main electrical panel. They are black and measure about 6 inches high x 5 inches wide x 2 1/2 inches deep. The units have a green LED "On" light, a red LED "Low Water" light and test and manual reset buttons on the top. "McDonnell and Miller," "Guard Dog," "Low Water Cut-Off" and model numbers 750-MT-120, 751-MT-120, 751P-MT-120 or 752P-MT-24 are printed on a white label on the outside of the unit. Date codes G41 or H41 are inked on the inside back plate.

CPSCOct 9, 2014Nationwide• Fluid Handling LLC, of Morton Grove, Ill., a division of Xylem Inc.

BD Insyte Autoguard Catheter (BD) - Potential Body Damage (2014)

BD Insyte Autoguard may have potential damage along the body of the catheter.

Class IIModerate

FDAOct 9, 2014Nationwide• Becton Dickinson & Company

MX 16-slice CT Scanner (Philips) - Image Orientation Problem (2014)

"The orientation of images is displayed incorrectly. When operator chooses gantry on the right side from operation console, and the patient position is HFDL, HFDR, FFDL or FFDR, the patient position picture and text is not consistent. "L" and "R" of scan images are reversed and this is not consistent with the patient actual position. "When a surview which is longe

Class IIModerate

FDAOct 9, 2014AR, CA, FL +17 more• Philips Medical Systems (Cleveland) Inc

Cesarean Pack (Customed) - Sterility Compromise (2014)

Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.

Class IHigh

FDAOct 8, 2014FL, NY, PR• Customed, Inc