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The Hershey Company

The Hershey Company Recalls

All product recalls associated with The Hershey Company.

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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 3501–3520 of 10393 recalls

Chocolate Shell Topping (Hershey's) – Mislabeled Product (2021)

Undeclared Allergen

The Hershey Company, 19 East Chocolate Avenue, Hershey PA 17033 is voluntarily recalling of a specific lot of Hershey s Chocolate Shell Topping in a 7.25-oz. (205g) bottle UPC (346000) after learning that 1,700 bottles were incorrectly filled with Heath Shell Topping which is made with almonds. Undeclared Allergen.

Class IHigh

FDAMay 5, 2021AZ, AR, CO +9 more• The Hershey Company

Atellica CH 930 Analyzer (Siemens) – Photometer Lamp Saturation (2021)

Photometer Lamp May Reach Saturation Without Flagging Results, may generate erroneously elevated or depressed patient results

FDAMay 4, 2021Nationwide• Siemens Healthcare Diagnostics, Inc.

Micardis Tablets (Boehringer) – Subpotent Drug (2021)

Subpotent Drug

1...174 175176177 178...520

Page 176 of 520Next

Class IIModerate

FDAMay 4, 2021AR, CO, CT +8 more• Boehringer Ingelheim Pharmaceuticals, Inc.

CT Fluoroscopy Ceiling Mount (Philips) – Monitor Bracket Wear (2021)

Significant wear of the Monitor Bracket Assembly shaft may go unrecognized could lead to the Monitor Bracket Assembly detaching from the Suspension Arm, and resulting in injury to patient, operator, bystander, or service person located in the path of a falling part

FDAMay 1, 2021Nationwide• Philips North America Llc

ACE Control Set (Sentinel) – Stability Requirements Issue (2021)

Claim for stability after reconstitution from lyophilized to liquid form does not meet the requirements. New IFU instructions for handling the product provided to end users.

FDAApr 30, 2021Nationwide• Sentinel CH SpA Via Robert Koch

4x6 Acidophilus Capsules (NOW) – undeclared ingredients (2021)

Undeclared Allergen

Foreign capsules included in bottle. Undeclared ingredients.

Class IIILow

FDAApr 28, 2021Nationwide• NOW Health Group Inc.

Leccurate SARS-CoV-2 Antibody Test (Lepu Medical) – Unauthorized Distribution (2021)

Leccurate SARS-CoV-2, Antibody Rapid Test Kit (Colloidal Gold Immunochromatography) is not authorized, cleared, or approved for marketing and/or distribution in the U.S.

FDAApr 26, 2021FL, GA, IL +2 more• LEPU MEDICAL TECHNOLOGY (BEIJING) CO., LTD Building 7-1 NO. 37 Chaoqian Rd; Changping Tech Zone Beijing China

Ingenia Ambition X (Philips) – Lifting Block Issue (2021)

The MR magnet is equipped with 4 lifting blocks, which are positioned on top of the magnet. These blocks are used to allow the magnets to be moved in or out by a lifting crane, e.g. during decommissioning or moving activities. A mechanical issue was detected on these hoisting interface blocks on top of the magnet.

FDAApr 23, 2021FL, GA, MI +8 more• Philips North America Llc

Ingenia Ambition S (Philips) – Lifting Block Issue (2021)

FDAApr 23, 2021FL, GA, MI +8 more• Philips North America Llc

Welmate Lidocaine Cream (Yash) – Packaging Issue (2021)

This recall involves Welmate Lidocaine Numbing Cream in a 113 g (4 oz.) white jar with a blue, orange and green label and a white cap. "Welmate," "5% Lidocaine," the Welmate logo and UPC code 373581105045 or 373581000012 are printed on the label. The lot numbers and corresponding expiration dates included in the recall are printed on the underside of the jar as follows: Lot Numbers Expiration Dates ELNC2001 05/2022 ELNC2002 05/2022 EL5C2001 11/2022 EL5C2002 11/2022 EL5C2101 11/2022 EL5C2102 11/2022

CPSCApr 22, 2021Nationwide• Yash Pharmaceuticals, of India

Centaur Syphilis Assay (Siemens) – Test Carryover (2021)

Potential for the ADVIA Centaur Syphilis assay to carryover into other commercial assays. This carryover effect only occurs when the impacted assays are used immediately following testing with the Syphilis assay on the ADVIA Centaur XP/XPT or ADVIA Centaur CP systems

FDAApr 21, 2021Nationwide• Siemens Healthcare Diagnostics, Inc

RayStation (RaySearch) – Clinical Goal Evaluation (2021)

Evaluation of a clinical goal for the voxelwise worst dose distributions may be misleading after editing the clinical goal. It also describes an issue with contouring when the spacing between slices is d 1 mm, present in RayStation/RayPlan versions from 6 up to 10A.

FDAApr 21, 2021Nationwide• RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden

Biopsy Needle (Innovative Tomography) – Sterility Concern (2021)

Sterility Assurance; Coaxial Interventional Needle labeled as sterile may not have been adequately sterilized

FDAApr 21, 2021Nationwide• INNOVATIVE TOMOGRAPHY PRODUCT GMBH Universitatsstr. 136 Bochum Germany

Rubber Dam Clamp (Dentech) – Part Breakage Risk (2021)

Removing parts for safety reasons due to possible breakage.

FDAApr 21, 2021Nationwide• Dentech Corp. 53 Shimizu-Cho, Itabashi-Ku Tokyo Japan

Interventional Needle (Innovative Tomography) – Sterility Concern (2021)

Sterility Assurance; Coaxial Interventional Needle labeled as sterile may not have been adequately sterilized

FDAApr 21, 2021Nationwide• INNOVATIVE TOMOGRAPHY PRODUCT GMBH Universitatsstr. 136 Bochum Germany

Acyclovir Tablets (Heritage) – missing lot details (2021)

Labeling: Incorrect or Missing Lot and/or Exp Date

Class IIILow

FDAApr 21, 2021OH• Heritage Pharmaceuticals Inc

Enterprise Viewer (Change Healthcare) – Image Style Defect (2021)

A software defect was identified where the Image Styles defined by presentation states from CHRS are not displayed in CHEV.

FDAApr 19, 2021Nationwide• CHANGE HEALTHCARE CANADA COMPANY

Innova IGS System (GE Healthcare) – Monitor Line Defect (2021)

The IGS system can experience a single vertical line defect where the vertical line divides and horizontally shifts live monitor images into two unequal image parts within the monitor display screen.

FDAApr 19, 2021Nationwide• GE Healthcare, LLC

Cardiac Assessment System (GE Healthcare) – Report Mismatch (2021)

If a certain sequence of events occur, the pdf test report that belongs to one patient will appear in a different patient's record when viewed in an Electronic Medical Record (EMR) or a similar system.

FDAApr 19, 2021Nationwide• GE Healthcare, LLC

Vitafusion Kids Melatonin 50ct (Church & Dwight) – Metallic Mesh (2021)

Potential presence of a metallic mesh material in products.

Class IIModerate

FDAApr 19, 2021Nationwide• Church & Dwight Co., Inc. OGI Distribution Center