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Sigma-Aldrich Mfg LLC

Sigma-Aldrich Mfg LLC Recalls

All product recalls associated with Sigma-Aldrich Mfg LLC.

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Recall Summary

Total Recalls

1000

Past Year

582

Class I (Serious)

Most Recent

Dec 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 8921–8940 of 10937 recalls

Sigma-Aldrich Mfg LLC: Sigma-Aldrich Histopaque-1077, Ref. 10771, packaged in 50...

Some of the product was contaminated with Pseudomonas mendocina

FDASep 4, 2009Nationwide• Sigma-Aldrich Mfg LLC

Medical Components, Inc dba MedComp: Medcomp, 10F Bioflex Tesio Kit with cutting trocar. Catal...

mislabeled as right are actually left

FDASep 2, 2009Nationwide• Medical Components, Inc dba MedComp

Hitachi Medical Systems America Inc: Hitachi Oasis Magnetic Resonance Scanners Software V1.0C ...

The device has a software error that could potentially lead to a misdiagnosis.

FDASep 1, 2009Nationwide• Hitachi Medical Systems America Inc

1...445 446447448 449...547

Page 447 of 547Next

Medtronic Neuromodulation: Medtronic Indura 1P Intrathecal Catheter, model 8709SC, M...

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.

FDAAug 27, 2009WA, PR• Medtronic Neuromodulation

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...

FDAAug 27, 2009WA, 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.

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.

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

GE Medical Systems, LLC: GE Healthcare Definium 8000.Model # 5131070. GE Healthcar...

Certain GE Radiographic fixed X-ray tables (Proteus XR/a, Revolution XR/d, and Definium 8000) were found to have tabletops that move unexpectedly in a bi-directional mode. In rare cases, a malfunction may occur, which could result in the tabletop brakes falling to engage when the control foot pedal is released to lock the floating tabletop in place.

FDAAug 13, 2009Nationwide• GE Medical Systems, LLC

GE Medical Systems, LLC: GE Healthcare Revolution XR/d. Model #'s 2259988-2 & 235...

FDAAug 13, 2009Nationwide• GE Medical Systems, LLC