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Frigidaire, a division of Electrolux Home Products Inc., of Augusta, Ga.

Frigidaire, a division of Electrolux Home Products Inc., of Augusta, Ga. Recalls

All product recalls associated with Frigidaire, a division of Electrolux Home Products Inc., of Augusta, Ga..

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Recall Summary

Total Recalls

1000

Past Year

893

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 14841–14860 of 17593 recalls

Smoothtop Electric Ranges (Frigidaire) – Fire Hazard (2009)

Fire/Burn Risk

This recall involves Frigidaire, Frigidaire Gallery, Frigidaire Professional and Kenmore Elite smoothtop electric ranges with rotary knobs and digital displays. The following model and serial numbers are included in the recall: Frigidaire (Serial Number Range VF122xxxxx - VF831xxxxx) and Models Beginning with FEFBZ90GC FEFLMC55GC FEFLZ87GC GLEF396AB GLEF396AQ GLEF396AS GLEF396CQ GLEF396CS GLEFM397DB GLEFM397DQ GLEFM397DS GLEFM97FPB GLEFM97FPW GLEFM97GPB GLEFM97GPW LEEFM389FE PLEF398AC PLEF398CC PLEF398DC PLEFM399DC PLEFMZ99EC PLEFMZ99GC PLEFZ398EC PLEFZ398GC Kenmore Elite (Serial Number Range VF122xxxxx - VF334xxxxx) and Models Beginning with 790.99012 790.99013 790.99014 790.99019 The model and serial number can be found by opening the range drawer at the base of the unit.

CPSCAug 27, 2009Nationwide• Frigidaire, a division of Electrolux Home Products Inc., of Augusta, Ga.

Medtronic Neuromodulation: Medtronic Intrathecal Catheter, model 8731SC, Method of S...

Current labeling for Medtronic Sutureless Connector (SC) catheters and revision kits (hereafter referred to as SC catheters) incorrectly states that SC catheters are compatible with Medtronic IsoMed constant-flow infusion pumps. SC catheters are compatible with Medtronic SynchroMed II and SynchroMed EL pumps. Medtronic has determined that SC catheters are not compatible with IsoMed pumps.

FDA

1...741 742743744 745...880

Page 743 of 880Next

Aug 27, 2009

WA, PR

• Medtronic Neuromodulation

Medtronic Neuromodulation: Medtronic Sutureless Pump Connector Revision Kit, model 8...

FDAAug 27, 2009WA, PR• Medtronic Neuromodulation

Medtronic Neuromodulation: Medtronic Intrathecal Catheter Pump Segment Revision Kit,...

FDAAug 27, 2009WA, PR• Medtronic Neuromodulation

Window Blinds (Vertical Land) – Strangulation Risk (2009)

This recall involves all Vertical Land custom-made vertical and cellular window coverings that do not have a cord tensioning device and horizontal blinds that do not have inner cord stop devices. A sticker identification label can be found on the head rail of some of the window coverings which lists the company's name, address and telephone number.

CPSCAug 26, 2009Nationwide• Vertical Land Inc., of Panama City Beach, Fla.

Roller Shades (VIMCO) – Strangulation Risk (2009)

This recall involves custom-ordered made-to-measure manual roller shades. The shades were sold in a variety of colors, fabrics, and sizes. They have a label on an adhesive strip that connects the shade fabric to the roller tube that reads "Lutron Shading Solutions" and "800-446-1503." The shade needs to be removed from the brackets and unrolled completely to access the label. The shade was sold with an orange, black and white hang tag warning consumers that "young children can STRANGLE in cord and bead chain loops." However, the hang tag may have been discarded upon installation. Nearly all shades were professionally installed.

CPSCAug 26, 2009Nationwide• Virginia Iron and Metal Company Inc. (VIMCO), of Ashland, Va.

Beckman Coulter Inc.: Synchron CX Immuno-Protein Cal, part number: 442840, ot...

A recall was initiated because Beckman has confirmed that the standardization of the Immuno Protein Calibrator Set has been re-established to IFCC Reference Preparation for Plasma Proteins, BCR-470 beginning with lot number M901330.

FDAAug 26, 2009Nationwide• Beckman Coulter Inc.

Smiths Medical Hythe Hythe, Kent United Kingdom: Portex Tracheal Tube, Cut to Length, Oral, Siliconized, 2...

Pediatric Trachel Tube manufactured with internal diameter smaller than indicated in the label may result in inability to remove secretions and cause partial or complete obstruction of the airway

FDAAug 25, 2009Nationwide• Smiths Medical Hythe Hythe, Kent United Kingdom

Smiths Medical Hythe Hythe, Kent United Kingdom: Portex Polar Preformed Tracheal Tube, South Oral, Murphy ...

Pediatric Trachel Tube manufactured with internal diameter smaller than indicated in the label may result in inability to remove secretions and cause partial or complete obstruction of the airway

FDAAug 25, 2009Nationwide• Smiths Medical Hythe Hythe, Kent United Kingdom

Smiths Medical Hythe Hythe, Kent United Kingdom: Portex Tracheal Tube, Oral/Nasal, Siliconized, 2.5 mm Pro...

Pediatric Trachel Tube manufactured with internal diameter smaller than indicated in the label may result in inability to remove secretions and cause partial or complete obstruction of the airway

FDAAug 25, 2009Nationwide• Smiths Medical Hythe Hythe, Kent United Kingdom

Medtronic Neuromodulation: Medtronic Enterra Therapy, Gastric Electrical Stimulation...

Medtronic is in the process of updating the Enterra Therapy labeling to include information regarding the risks of bowel obstruction and/or perforation. Medtronic has received 15 reports since November 2002 of bowel obstruction and/or perforation of the bowel associated with Enterra Therapy System leads. Of the 15 reported events, 11 required surgical intervention (all patients recovered withou

FDAAug 25, 2009Nationwide• Medtronic Neuromodulation

Smiths Medical Hythe Hythe, Kent United Kingdom: Portex Uncuffed Paediatric Sized Tracheal Tube, Oral Nasa...

Pediatric Trachel Tube manufactured with internal diameter smaller than indicated in the label may result in inability to remove secretions and cause partial or complete obstruction of the airway

FDAAug 25, 2009Nationwide• Smiths Medical Hythe Hythe, Kent United Kingdom

Entertainment Stands (Ameriwood) – tip-over risk (2009)

This recall involves Your Zone Loft Collection entertainment stands. The stands are intended to be used as gaming centers. The recall includes Autumn Beech YZ084-104-13-19 stands with model number 1156020WY. Model information is printed on the instruction manual.

CPSCAug 25, 2009Nationwide• Ameriwood Industries, of Wright City, Mo.

Acumed LLC: Biotrak PLLA Pin, Resorbable Fixation System, Biotrak 20 ...

Labeling may contain 2 lot numbers and 2 model numbers. It was observed that the box top label (30170060-S, W67391) does not match the two side labels (3010320-S, W67385). The part and patient labeling inside the box match the side labels (30170320-S, W67385).

FDAAug 21, 2009Nationwide• Acumed LLC

Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals: AccuSure, U-100, 31Gauge, 1cc Insulin Syringe, 5/16" (8mm...

Needles separate from the barrels of the syringes

FDAAug 21, 2009Nationwide• Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals

Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals: AccuSure, U-100, 31Gauge, 1/2cc Insulin Syringe, 5/16" (8...

Needles separate from the barrels of the syringes

FDAAug 21, 2009Nationwide• Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals

Dust Collection Switches (Woodstock) – fire hazard (2009)

Fire/Burn Risk

The recalled product is a remote dust collector switch, which remotely turns on and off a woodworking dust collector. The product is a black electrical outlet box that comes with two hand-held remote controls. The electrical outlet box has a label that reads "Remote Dust Collector Switch". Both the electrical box and remote controls have "Shop Fox" molded into the plastic on the top side of the product. Model numbers D3038 & D3346 were printed on the carton but not on the remote control unit. The recalled switches measure 4 and 13/16" long by 3 and 7/16" wide.

CPSCAug 18, 2009Nationwide• Woodstock International, of Bellingham, Wash.

Gyrus ACMI Corporation: Gyrus ACMI PKS Seal Open Forceps, model 3103PK, 9-3/4" cu...

Gyrus ACMI received complaints of a problem with 3103PK, 3104PK, 3105PK, 915000PK, 915005PK, 915010PK - Gyrus ACMI PKS Seal Open Forceps. The metal shim between the jaws may detach during the procedure and fall into the surgical field. The detached shim may be undetected and be left behind in the patient. This circumstance could subsequently cause complications. Further use of this product should cease, affected product should be removed from stockrooms and returned to Gyrus ACMI.

FDAAug 18, 2009PR• Gyrus ACMI Corporation

Gyrus ACMI Corporation: Gyrus ACMI PKS Seal Open Forceps, model 3104PK, 9-3/4" st...

FDAAug 18, 2009PR• Gyrus ACMI Corporation

Gyrus ACMI Corporation: Gyrus ACMI PKS Seal Open Forceps, model 915010PK, 9-3/4" ...

FDAAug 18, 2009PR• Gyrus ACMI Corporation