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Corin Ltd Unit 1-57-8 Corinium Centre Cirencester United Kingdom

Corin Ltd Unit 1-57-8 Corinium Centre Cirencester United Kingdom Recalls

All product recalls associated with Corin Ltd Unit 1-57-8 Corinium Centre Cirencester United Kingdom.

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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 5021–5040 of 17593 recalls

Corin TriFit TS (Corin) – Stem Labeling Mixup (2021)

Units from one batch of TriFit TS size 2 stem were found to be labeled as a TriFit CF size 7 stem. And vice versa.

Moderate

FDAMay 6, 2021Nationwide• Corin Ltd Unit 1-57-8 Corinium Centre Cirencester United Kingdom

Pecan Halves (South Georgia Pecan) – peanut contamination (2021)

The firm received complaints of peanuts in their cases of pecans.

Class IIModerate

FDAMay 6, 2021MI• South Georgia Pecan Company

Sweet Apple Cider (Kauffman's) – elevated patulin (2021)

Product contains elevated levels of patulin.

Class IIModerate

1...250 251252253 254...880

Page 252 of 880Next

FDA

May 6, 2021

MD, NJ, PA +1 more

• A L Kauffman & Sons Co. DBA Kauffman's Fruit Farm and Market

WorkMate Claris Upgrade Kit (Abbott) – Software Functionality Loss (2021)

Due to a software error, the user may lose functionality of the system or the screen may turn black during operation.

Moderate

FDAMay 5, 2021Nationwide• Abbott Laboratories Inc. (St Jude Medical)

WorkMate Claris Upgrade Kit (Abbott) – Software Functionality Loss (2021)

Due to a software error, the user may lose functionality of the system or the screen may turn black during operation.

Moderate

FDAMay 5, 2021Nationwide• Abbott Laboratories Inc. (St Jude Medical)

Omnera 400A Radiographic System (Arcoma) – Liquid Ingress Risk (2021)

There is the potential for the X-Ray system to short circuit due to an ingress of liquid in the display handles which may result in uncontrolled movement of the Overhead Tube Crane (OTC).

High

FDAMay 5, 2021Nationwide• Arcoma AB Annavagen

Omnera 400T Radiographic System (Arcoma) – Liquid Ingress Risk (2021)

There is the potential for the X-Ray system to short circuit due to an ingress of liquid in the display handles which may result in uncontrolled movement of the Overhead Tube Crane (OTC).

High

FDAMay 5, 2021Nationwide• Arcoma AB Annavagen

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

Arcimoto Roadster (Arcimoto) – Communication Software Error (2021)

Arcimoto Inc (Arcimoto) is recalling certain 2019-2021 FUV, 2021 Rapid Responder, 2020 Deliverator, 2020-2021 Roadster. Due to a software error, communication between inverters may time out, possibly resulting in an unexpected battery shutdown.

Moderate

NHTSAMay 4, 2021Nationwide• ARCIMOTO

Arcimoto FUV (Arcimoto) – Seat Belt Retractor Defect (2021)

Arcimoto Inc (Arcimoto) is recalling certain 2019-2021 FUV, 2020 Deliverator, 2021 Rapid Responder motorcycles. The seat belt retractor spool sleeve may be cracked, allowing broken pieces to block the seat belt from retracting.

Moderate

NHTSAMay 4, 2021Nationwide• ARCIMOTO

Arcimoto FUV (Arcimoto) – Steering Arm Defect (2021)

Arcimoto Inc (Arcimoto) is recalling certain 2019-2021 FUV, 2020 Deliverator, 2020-2021 Roadster, and 2021 Rapid Responder motorcycles. The Steering Angle Sensor (SAS) may have been incorrectly calibrated, causing the SAS to fail to or incorrectly detect a fault.

Moderate

NHTSAMay 3, 2021Nationwide• ARCIMOTO

Shrayy White Chalk (A Life African Market) – Lead Contamination (2021)

Product contains elevated levels of lead and arsenic.

Class IIModerate

FDAMay 3, 2021DE, MA, NY +1 more• A LIFE AFRICAN MARKET CORP

Synapse Cardiovascular Software (Fujifilm) – Patient ID Reuse (2021)

Laceration Risk

Software versions 6.0.4 to 6.2.1 using Advanced Reporting -possibility that a previously assigned internal patient database ID can be reused for a new patient. It was discovered that this value does not increase when a patient merge activity is executed in a specific sequence

Moderate

FDAApr 30, 2021Nationwide• Fujifilm Medical Systems U.S.A., Inc.