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Southern Living At Home, of Birmingham, Alabama

Southern Living At Home, of Birmingham, Alabama Recalls

All product recalls associated with Southern Living At Home, of Birmingham, Alabama.

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Recall Summary

Total Recalls

1000

Past Year

295

Class I (Serious)

116

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 4141–4160 of 4465 recalls

Glass Votive Candle Holders – Potential Risk (2005)

This recall involves the Old Taylor Estate Candelier with item number 40697 (the item number is located on one side and the top of each box). The chandeliers have eight glass votive candle holders. Old Taylor Estate Candeliers purchased after September 2005 are not included in this recall.

CPSCNov 17, 2005Nationwide• Southern Living At Home, of Birmingham, Alabama

Abbott Spine: SC-AcuFix Core Instruments Surgical Techniques covering S...

Modification to labeling for surgical implant.

FDANov 14, 2005Nationwide• Abbott Spine

Abbott Laboratories Diagnostic Div: Clinical Chemistry Immunoglobulin M, List Number 1E01-20

These specific protein assays are not meeting the 57-day on board stability claim

FDA

1...206 207208209 210...224

Page 208 of 224Next

Nov 10, 2005

Nationwide

• Abbott Laboratories Diagnostic Div

Abbott Laboratories Diagnostic Div: Clinical Chemistry Prealbumin, List Number 1E02-20

These specific protein assays are not meeting the 57-day on board stability claim

FDANov 10, 2005Nationwide• Abbott Laboratories Diagnostic Div

Abbott Laboratories Diagnostic Div: Clinical Chemistry Apolipoprotein A1, List Number 9D92-20

These specific protein assays are not meeting the 57-day on board stability claim

FDANov 10, 2005Nationwide• Abbott Laboratories Diagnostic Div

Abbott Spine: TraXis Vue Spinal Implant System, Part #2601-090921

Implants were manufactured without radiographic markers.

FDANov 2, 2005Nationwide• Abbott Spine

Boston Scientific Corporation One Boston: Boston Scientific Scimed Maverick 2 Monorail 12mm Balloon...

Two lots may not be correctly labeled. Specifically , a 2.5 mm x 12 mm unit was incorrectly labeled as a 3.5 x 20 mm unit on the box and tyvek label.

FDANov 1, 2005Nationwide• Boston Scientific Corporation One Boston

Abbott Molecular: Vysis LSI p16 (9p21)/CEP 9 (9p11-q11) Dual Color Probe Se...

The DNA-Probe has a target size of ~300 Kb region instead of the labeled ~190 Kb region.

FDAOct 28, 2005Nationwide• Abbott Molecular

Musical Bells Christmas Trees (Cracker Barrel) – defective item (2005)

Fire/Burn Risk

These battery-operated Miniature Musical Bells Christmas Trees have the item number 233010. The tree is about 18 inches high and 8 inches wide with three tiers of bells and a lighted star at the top. Each tree has "Made in China" embossed on the bottom. The trees use eight "AA" 1.5-volt batteries.

CPSCOct 20, 2005Nationwide• Cracker Barrel Old Country Store®, of Lebanon, Tenn.

Abbott Laboratories MPG: ARCHITECT STAT Myoglobin Calibrators; list 02K43-01; each...

Some of the kits were shipped at the incorrect shipping temperature. They were shipped ambient, but should have been shipped frozen.

FDAOct 17, 2005KY, MT, PA +2 more• Abbott Laboratories MPG

Bombardier Outlander 800 ATV – Mechanical Risk (2005)

The recalled vehicles are model year 2006 Outlander 800 H.O. XT Bombardier ATVs. The model numbers affected are 2J6A and 2J6E. The model numbers are located in the serial number on the identification sticker under the seat. The ATVs have the words, "Bombardier" and "Rotax 800" on the fenders.

CPSCOct 11, 2005Nationwide• Bombardier Recreational Products Inc., of Valcourt, Providence of Quebec, Canada

Abbott Laboratories: Fleixiflo Quantum Enteral Pump.

Pumps have the potential to malfunction and result in a significant over-under delivery of enteral formula.

FDAOct 7, 2005AL, CA, IN +12 more• Abbott Laboratories

Abbott Laboratories: Abbott brand CELL-DYN 1800 DILUENT Packaged in 3.8L conta...

The product failed 12-month stability testing that can lead to falsely reduced hemoglobin (Hgb) test results.

FDASep 20, 2005IN, OR• Abbott Laboratories

Robertshaw Gas Control Valves – Mechanical Risk (2005)

Fire/Burn Risk

The R110 Gas Control Valves being recalled are installed on natural and liquid propane (LP) gas water heaters. The recalled valves were manufactured between July 25, 2005 and August 14, 2005 with production date codes 5-31 through and including 5-33, although not all valves with these date codes are affected. The recalled valves were installed on the following water heater brands: American Proline, Bradford White, GE, GSW, Hotpoint, Jetglas, John Wood, Lochinvar, Premier Plus, Powerflex, Rheem, Richmond, Ruud, Vanguard, Whirlpool, and U.S. Craftmaster. The model and serial number can be found on the manufacturer's label on the water heater. Electric water heaters are not included.

CPSCSep 16, 2005Nationwide• Robertshaw Controls Co., of Long Beach, Calif.

B. Braun Medical, Inc.: D-Stat Dry Hemostatic Bandage. The product is an adhesive...

package sealing defect - product may not be sterile

FDASep 15, 2005AZ, CA, FL +13 more• B. Braun Medical, Inc.

Abbott Laboratories, Inc: ARCHITECT c8000 Analyzer System Processing Module, a full...

Software deficiency causing potential shift in absorbance readings for test results.

FDASep 14, 2005Nationwide• Abbott Laboratories, Inc

B. Braun Medical, Inc.: 7F Locking Tearaway Introducers non-sterile. Part number ...

Tear away sheath assembly may contain a sheath (8FR) that is not the correct French size for the dilator (7FR).

FDASep 1, 2005Nationwide• B. Braun Medical, Inc.

Abbott Diabetes Care, Inc.: FreeStyle CoPilot Web Based Data Management System, and F...

Downloadable software obtained from the firm's website displays user data (including but not limited to insulin levels and pump statistics data) in a matter that may be misinterpreted and result in mistreatment of therapy.

FDAAug 30, 2005OR• Abbott Diabetes Care, Inc.

Stork Craft Toy Boxes (Stork Craft) – Manufacturing Flaw (2005)

The recall includes toy boxes with manufacture date codes between November 2002 and July 2004 and the following model numbers and colors: 01520-331 - white, 01520-334 - cherry, 01520-33C - cognac, 01520-33L - oak, and 01520-33N - natural. The manufacture date codes, model numbers, and colors are located on a label underneath the toy boxes. The toy boxes measure 27 inches long by 18 inches wide and 17 inches high. The boxes are constructed of pine.

CPSCAug 19, 2005Nationwide• Stork Craft Manufacturing Inc., of Richmond, British Columbia, Canada

Boston Scientific Corporation One Boston: Renegade Hi-Flo Microcatheter Kits, Catalog/Order # 18-29...

Outer box of the product may have an incorrect expiration date listed as 2007-06, while the correct expiration date is 2007-04

FDAAug 10, 2005KY, TX• Boston Scientific Corporation One Boston