Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Whirlpool Corporation World Headquarters Benton

Whirlpool Corporation World Headquarters Benton Recalls

All product recalls associated with Whirlpool Corporation World Headquarters Benton.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

589

Class I (Serious)

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 4201–4220 of 10393 recalls

PAPR (Powered Air-Purifying Respirator) - Model# WLPAPR20W1 (Whirlpool Corporation World Headquarters Benton) – the rivets that secure the elastic he... (2020)

The rivets that secure the elastic headband to the face shield have the potential to be mis-assembled. When this condition occurs, it can result in a headband that can become loose from face shield allowing the face shield to shield on the user.

FDAJul 2, 2020MI• Whirlpool Corporation World Headquarters Benton

DCA Vantage Scanner (Siemens) – Barcode Verification Issue (2020)

If DCA Vantage Analyzer is configured to run Code 39 with check digit, the scanner is not confirming the integrity of read barcode data using the check digit. Also, if DCA Vantage Analyzer is configured to run Code 39 with check digit and an operator erroneously scans a Code 39 barcode without a check digit, the scanner incorrectly sends the code and the last character is removed.

FDAJun 30, 2020Nationwide• Siemens Healthcare Diagnostics, Inc.

IntelliVue MX800 Monitor (Philips) – Defective Power Supply (2020)

1...209 210211212 213...520

Page 211 of 520Next

Some Intellivue MX700/MX800 Patient Monitors were delivered with defective power supplies. The defective power supplies might energize the metal parts of monitor if the grounding instructions were not followed, and may also cause the monitor to stop operating or prevent it from being switched on.

FDAJun 30, 2020CA, HI, MA +2 more• Philips North America, LLC

Spectrum IQ Infusion System (Baxter) – Cleaning Practices Update (2020)

Baxter is updating the device IFU for safety communication regarding cleaning practices.

FDAJun 30, 2020Nationwide• Baxter Healthcare Corporation

IntelliVue MX700 Monitor (Philips) – Defective Power Supply (2020)

FDAJun 30, 2020CA, HI, MA +2 more• Philips North America, LLC

SIGMA Spectrum Infusion Pump (Baxter) – Cleaning Practices Update (2020)

Baxter is updating the device IFU for safety communication regarding cleaning practices.

FDAJun 30, 2020Nationwide• Baxter Healthcare Corporation

PeriLoc Targeter (Smith & Nephew) – Incorrect Hand Marking (2020)

The 4.5MM PeriLoc Targeter right hand part was anodized green and was marked as a left-hand part.

FDAJun 29, 2020Nationwide• Smith & Nephew, Inc.

IntelliVue G7m Gas Module (Philips) – Measurement Interruption (2020)

The device may experience an interruption of gas measurement due to a firmware issue, ceasing measurement and display of gas levels and generating one or more technical or INOP alarms.

FDAJun 25, 2020Nationwide• Philips North America, LLC

Garlic Shrimp Poke (HKH JVC) – Listeria Contamination (2020)

Listeria

Potential Listeria monocytogenes contamination.

Class IHigh

FDAJun 25, 2020HI• HKH JVC LLC.

SutureFixx Ultra (Smith & Nephew) – Drill Size Packaging Error (2020)

A packaging error resulted in a XL drill being presented for use instead of the S drill. The XL drill is one inch longer than the S drill.

FDAJun 24, 2020AL, AZ, AR +20 more• Smith & Nephew, Inc.

TRIGEN Intramedullary Nail (Smith & Nephew) – Sterilization Issue (2020)

A manufacturing error which resulted in the re-sterilization of the ultra-high-molecular-weight polyethylene (UHMWPE) sleeve.

FDAJun 24, 2020IN• Smith & Nephew, Inc.

Smith & Nephew T-Fix Drill Pac (Smith & Nephew) – Sleeve Shortage (2020)

The T-Fix sterile package contains only one sleeve instead of two, The device will not perform as intended for the second bone tunnel due to the absence of thesleeve

FDAJun 24, 2020Nationwide• Smith & Nephew, Inc.

Neurosign V4 Monitor (Magstim) – Cable Connection Risk (2020)

Reports that manipulation of the cable which connects the pre-amplifier to the nerve monitor, and the cable which connects the pre-amplifier to the stimulator pod, may cause damage to the internal construction of the cables.

FDAJun 23, 2020MN• The Magstim Company Limited Spring Gardens Whitland United Kingdom

TTDEYE Devil Red Lens (TTDEYE) – Unauthorized Distribution (2020)

Colored contact lenses were distributed without FDA clearance.

FDAJun 23, 2020Nationwide• Chengdu Ai Qin E-commerce Co., Ltd N0.200, Tian Fu Fifth Street Gao Xin China

TTDEYE Radial Pink Lens (TTDEYE) – Unauthorized Distribution (2020)

Colored contact lenses were distributed without FDA clearance.

FDAJun 23, 2020Nationwide• Chengdu Ai Qin E-commerce Co., Ltd N0.200, Tian Fu Fifth Street Gao Xin China

Sutter Swyng Forceps (Sutter) – Labeling Inconsistency (2020)

The label on the cardbox and the blister show the correct symbols for sterilization using irradiation and storage at 5 C to 40 C, the package insert (IFU) is labelled incorrectly. It shows the symbol for sterilization using Ethylene Oxide with the description for sterilization using irradiation.

FDAJun 23, 2020Nationwide• Sutter Medizintechnik GmbH Tullastr. 87 Freiburg Im Breisgau Germany