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
/
Getinge Group Logistics America, LLC

Getinge Group Logistics America, LLC Recalls

All product recalls associated with Getinge Group Logistics America, LLC.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

579

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 3541–3560 of 10937 recalls

CM320 Washer Disinfector (Getinge) – Hose Connection Defect (2020)

Fire/Burn Risk

The potential that the plastic inlet hose connections may deform or break as a result of material fatigue and/or over tightening of the clamps. A broken hose connection may lead to a hazardous situation of water leakage or water spray. The water leakage or water spray may result in a burn to the user and/or an inconvenience due to a procedural delay if the Washer Disinfector is taken out of service.

High

FDADec 21, 2020Nationwide• Getinge Group Logistics America, LLC

Harmony Referral System (Topcon) – Patient ID Mismatch (2020)

Harmony RS integrations with Topcon equipment, TRC NW-400 and the Signal Camera, allowed user input of non-unique patient IDs that caused multiple patient records and images to be combined under the first generated record

Moderate

FDADec 18, 2020AZ, MO, NY +3 more• Topcon Medical Systems, Inc.

Spud-Queen Lattice Cut Frozen Potatoes (JR Simplot) – Undeclared Wheat (2020)

1...176 177178179 180...547

Page 178 of 547Next

Undeclared Gluten

Undeclared wheat.

Class IHigh

FDADec 18, 2020AL, IN, MS• JR Simplot Company - Headquarters

Otis and CemcoLift Residence Elevators (Otis) – Entrapment Hazard (2020)

This recall involves Otis private residence elevators purchased before 2012 and CemcoLift private residence elevators purchased from 1999 to 2012. The elevators are used in consumers' homes.

Very High

CPSCDec 17, 2020Nationwide• Otis Elevator Company of Farmington, Ct.

Synapse PACS Software (Fujifilm) – Measurement Update Problem (2020)

The software does not update measurements and calculations in the Clinical Reporting Application (CRA) when the ventricular trace is changed in the study by a different user.

Moderate

FDADec 11, 2020Nationwide• Fujifilm Medical Systems U.S.A., Inc.

Outshine Fruit & Cream Bars (Dreyers) – Foreign Material (2020)

Firm received complaints of foreign material in ice cream bars.

Class IIModerate

FDADec 11, 2020MA, MI, NH +2 more• Dreyers Grand Ice Cream, Inc.

Homfa Cabinets (Shenzhen Luosi Ge) – Tip-Over Risk (2020)

This recall involves the Homfa HPB-087 and HPB-106 cabinets. The HPB-087 was sold in walnut brown and the HPB-106 was sold in wood grain. The cabinets measure about 29.75 inches tall, 31.5 inches wide, and 15.4 inches deep and weigh about 59 pounds.

High

CPSCDec 10, 2020Nationwide• Shenzhen Luosi Ge Trading Co., of China (owner of Homfa trademark)

Western Chief Toddler Boots – Choking Hazard (2020)

Choking Hazard

This recall includes the Western Chief "Abstract Camo," "Alia Silver," and "Sweetheart Navy" Light-Up Rain Boots in sizes 5-12 for toddlers or children. The recalled boots are camouflage, silver glitter, and navy with hearts; include boot handles; and have a light up feature in the heel of the boot. The rivets used to attach the handles are silver-gray in color. "Western Chief" and the model numbers are located on the inside tag of the boot. The recalled model numbers are T24121725P, T24121728P, and T24121729P.

Moderate

CPSCDec 9, 2020Nationwide• Washington Shoe Company, of Kent, Wash.

Auryxia (Akebia Therapeutics) – manufacturing deviation (2020)

CGMP Deviations

Class IIModerate

FDADec 9, 2020Nationwide• Akebia Therapeutics dba Keryx Biopharmaceutials, Inc

Regional Block Needles (BD) – Instructions Update (2020)

BD was advised by the European Notified Body, NSAI, that the instructions for use (IFU) needs to be updated to include the general contraindications

Moderate

FDADec 9, 2020AL, CT, FL +15 more• Becton Dickinson & Company

Stimex Insulated Needle (BD) – Instructions Update (2020)

BD was advised by the European Notified Body, NSAI, that the instructions for use (IFU) needs to be updated to include the general contraindications

Moderate

FDADec 9, 2020AL, CT, FL +15 more• Becton Dickinson & Company

Canon Interventional Angiography System (Canon) – Table Tilt Fault (2020)

System table may tilt because the bolts that fasten the vertical column and the table top tilting drive unit may become loose.

High

FDADec 8, 2020Nationwide• Canon Medical System, USA, INC.

Neurosign 100 (Magstim) – Mains Configuration Problem (2020)

A small number of Neurosign 100 Intraoperative Nerve Monitors may have been dispatched without being configured appropriately for the supply mains within the target Country. The specific deficiency includes: 1. Onboard voltage selector set to 240V (European Standard), versus 120V requirement for the United States and Canada. 2. Fuses installed in the Power Entry Module (PEM) 2xT315mAL (240V Standard), versus the 2xT630mAL requirement for a 120V mains supply.

Low

FDADec 8, 2020MN, NY, NC• The Magstim Company Limited Spring Gardens Whitland United Kingdom

Imatinib Mesylate Tablets (Shilpa Medicare) – manufacturing deviation (2020)

CGMP Deviations

Class IIModerate

FDADec 8, 2020Nationwide• Shilpa Medicare Limited

Azacitidine Injection (Shilpa Medicare) – CGMP Issues (2020)

CGMP Deviations

Class IIModerate

FDADec 8, 2020Nationwide• Shilpa Medicare Limited

Busulfan Injection (Shilpa Medicare) – CGMP Issues (2020)

CGMP Deviations

Class IIModerate

FDADec 8, 2020Nationwide• Shilpa Medicare Limited

Imatinib Mesylate Tablets (Shilpa Medicare) – CGMP Issues (2020)

CGMP Deviations

Class IIModerate

FDADec 8, 2020Nationwide• Shilpa Medicare Limited

Docetaxel Injection (Shilpa Medicare) – CGMP Issues (2020)

CGMP Deviations

Class IIModerate

FDADec 8, 2020Nationwide• Shilpa Medicare Limited

Azacitidine Injection (Shilpa Medicare) – CGMP Issues (2020)

CGMP Deviations

Class IIModerate

FDADec 8, 2020Nationwide• Shilpa Medicare Limited

IOLMaster 700 (Carl Zeiss) – Patient Data Transfer Issue (2020)

When using software 1.90.2.09 or 1.90.8.06 and using modality worklist functionality for patient data transfer, the selection of the patient in the patient list may not match the patient information displayed on the right side of the screen

High

FDADec 7, 2020AL, AZ, AR +36 more• Carl Zeiss Meditec AG Carl-Zeiss-Promenade 10 Jena Germany