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GE Medical Systems, LLC

GE Medical Systems, LLC Recalls

All product recalls associated with GE Medical Systems, LLC.

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Recall Summary

Total Recalls

1000

Past Year

891

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 3401–3420 of 17593 recalls

Centricity PACS-IW (GE Medical) – Hidden Studies (2022)

There is the potential that after installation of the IAS tool, some studies can remain hidden without user notification. Access to those hidden studies requires GE Healthcare assistance, which can result in a delay in reading the study.

Moderate

FDAOct 28, 2022Nationwide• GE Medical Systems, LLC

Kalera Krunch Lettuce - salmonella risk (2022)

Salmonella

Potential contamination with Salmonella

Class IHigh

FDAOct 28, 2022Nationwide• Kalera Public Limited Company

Kalera Butter Lettuce - salmonella risk (2022)

Salmonella

Potential contamination with Salmonella

1...169 170171172 173...880

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Class IHigh

FDAOct 28, 2022Nationwide• Kalera Public Limited Company

Kalera Baby Romaine Lettuce - salmonella risk (2022)

Salmonella

Potential contamination with Salmonella

Class IHigh

FDAOct 28, 2022Nationwide• Kalera Public Limited Company

CytoCell BCL11B Distal (Cytocell) – Chromomap Error (2022)

An error with the chromomap on version 1 of the package insert which is incorrect. The nucleotide locations specified in the insert are correct but the map has been created using the wrong coordinates.

Moderate

FDAOct 27, 2022TX• Cytocell Ltd. 418 Cambridge Science Park, Milton Road Oxford Gene Technology Cambridge United Kingdom

CytoCell BCL11B Proximal (Cytocell) – Mislabeling (2022)

Device is mislabeled. The package insert for this ASR device contains a chromomap - an image showing the position the FISH probe maps to on the specific chromosome. For this device the chromomap in version 1 of the package insert is incorrect and doesn't not match the probe design or specification contained on the package insert

Low

FDAOct 27, 2022TX• Cytocell Ltd. 418 Cambridge Science Park, Milton Road Oxford Gene Technology Cambridge United Kingdom

Cedar Creek Caramel Popcorn - gluten mislabeling (2022)

Label contains "Gluten Free" claim but product contains wheat and barley which are declared on the label.

Class IIModerate

FDAOct 27, 2022AZ, GA, IN +5 more• Rieckhoff Family Businesses, Inc dba Cedar Creek Popcorn

Pine-Sol Multi-Surface Cleaner (Clorox) – contamination risk (2022)

This recall involves Pine-Sol Scented Multi-Surface Cleaners in Lavender Clean, Sparkling Wave, and Lemon Fresh scents, CloroxPro Pine-Sol All Purpose Cleaners, in Lavender Clean, Sparkling Wave, Lemon Fresh, and Orange Energy scents, and Clorox Professional Pine-Sol Lemon Fresh Cleaners, with date codes beginning with the prefix "A4" and followed by a five-digit number less than 22249. The products are sold in bottles of 28, 48, 60, 100, 144, and 175 fluid ounces. In an abundance of caution, Clorox is recalling all of the above-described products manufactured at its Forest Park, Georgia facility through September 2022.

Moderate

CPSCOct 25, 2022Nationwide• The Clorox Company, of Oakland, California

Zingerman's Pumpkin Gelato (Zingerman's) – undeclared egg (2022)

Undeclared Egg

undeclared egg

Class IHigh

FDAOct 24, 2022MI• Zingerman's Creamery, LLC

Zingerman's Paw Paw Gelato (Zingerman's) – undeclared egg (2022)

Undeclared Egg

undeclared egg

Class IHigh

FDAOct 24, 2022MI• Zingerman's Creamery, LLC

Can-Am Ryker (Can-Am) – Electrical Harness (2022)

Bombardier Recreational Products (BRP) is recalling certain 2019-2023 Ryker motorcycles. The position light and flasher electrical harnesses in the front fenders may loosen and rub on the tire, leading to a short circuit and resulting in an engine stall while driving.

Moderate

NHTSAOct 22, 2022Nationwide• CAN-AM

Chicken Salad Sandwich Tray (Albertsons) – undeclared cashews (2022)

Store printed label on products does not include Tree Nuts (Cashews) in the ingredient statement and the contains statement.

Class IHigh

FDAOct 17, 2022CO, NE, NM +2 more• Albertsons Companies LLC

ReadyMeals Chicken Salad Quad (Albertsons) – undeclared cashews (2022)

Store printed label on products does not include Tree Nuts (Cashews) in the ingredient statement and the contains statement.

Class IHigh

FDAOct 17, 2022CO, NE, NM +2 more• Albertsons Companies LLC

U-Line Outdoor Freezers – fire hazard (2022)

Fire/Burn Risk

This recall involves U-Line Outdoor Series 24-inch Built-In Convertible Freezers with model number U-1224FZRSOD-00A and manufactured between 2017-2018. They have serial number ranges between 1745627020001-1745627020009; 1746096040001-1746096040077; 1850469050001-1850469050003; and 1850469059001-1850469059003. The model number, serial number, and "U-Line" brand name are printed on a plate located in the top right interior of the unit.

High

CPSCOct 13, 2022Nationwide• U-Line Corporation, of Milwaukee, Wisconsin

Superion Decompression System (Boston Scientific) – Weld Breakage Risk (2022)

Due to Indirect Decompression System devices exhibiting a potential for weld breakage at the spindle cap-to-main body interface. As a result of the separation of the spindle cap from the main body it may prevent proper deployment of the device during implantation.

Moderate

FDAOct 12, 2022Nationwide• Boston Scientific Neuromodulation Corporation

Basin Set (American Contract) – Labeling Mismatch (2022)

Basin Set labeling error: components within the kit are for the Single Basin Set. Therefore, the contents of the package do not match the contents listed on the label.

Low

FDAOct 12, 2022Nationwide• American Contract Systems, Inc.

BD Nexiva IV Catheter (Becton Dickinson) – Shield Separation Risk (2022)

During needle withdrawal, the tip shield may prematurely separate from the catheter adapter and preventing the needle tip from being in the safely shielded (leaving the needle tip exposed).

Moderate

FDAOct 12, 2022FL, GA, IL +10 more• Becton Dickinson Infusion Therapy Systems Inc.

PAJUNK Epidural Tray (Pajunk) – Medication Labeling Error (2022)

The tray contains a 2ml ampule of 0.75% Marcaine Spinal in lieu of a 10ml ampule of 0.9% Sodium Chloride as intended,.

Moderate

FDAOct 10, 2022Nationwide• Pajunk Medical Systems, L.P.

Papaverine Phentolamine Injection (Vital Care) – Sterility Risk (2022)

Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.

Class IIModerate

FDAOct 7, 2022AL, LA, MS +1 more• Pharmacy Plus, Inc. dba Vital Care Compounder

Acetylcysteine Ophthalmic Solution (Vital Care) – sterility concerns (2022)

Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.

Class IIModerate

FDAOct 7, 2022AL, LA, MS +1 more• Pharmacy Plus, Inc. dba Vital Care Compounder