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Champlain Chocolate Company

Champlain Chocolate Company Recalls

All product recalls associated with Champlain Chocolate Company.

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Recall Summary

Total Recalls

1000

Past Year

123

Class I (Serious)

Most Recent

Nov 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 881–900 of 2383 recalls

Basket Country Bunny ORG (Champlain Chocolate) - Undeclared Almonds (2021)

Undeclared Allergen

Product potentially contains undeclared almonds.

Class IIModerate

FDAApr 14, 2021CA, CT, MA +6 more• Champlain Chocolate Company

DONJOY UltraSling Pro (DJ Orthopedics) – Rivet Failure Risk (2021)

failed rivet at the chafe tab of arm sling.

FDAApr 12, 2021Nationwide• DJ Orthopedics de Mexico S.A. de C.V. Carretera Libre Tijuana-Tecate 20230 Submetropoli El Florido Tijuana Mexico

DONJOY UltraSling Pro (DJ Orthopedics) – Rivet Failure Risk (2021)

failed rivet at the chafe tab of arm sling.

1...43 444546 47...120

Page 45 of 120Next

FDA

Apr 12, 2021

Nationwide

• DJ Orthopedics de Mexico S.A. de C.V. Carretera Libre Tijuana-Tecate 20230 Submetropoli El Florido Tijuana Mexico

DONJOY UltraSling Pro (DJ Orthopedics) – Rivet Failure Risk (2021)

failed rivet at the chafe tab of arm sling.

FDAApr 12, 2021Nationwide• DJ Orthopedics de Mexico S.A. de C.V. Carretera Libre Tijuana-Tecate 20230 Submetropoli El Florido Tijuana Mexico

DONJOY UltraSling Pro (DJ Orthopedics) – Rivet Failure Risk (2021)

failed rivet at the chafe tab of arm sling.

FDAApr 12, 2021Nationwide• DJ Orthopedics de Mexico S.A. de C.V. Carretera Libre Tijuana-Tecate 20230 Submetropoli El Florido Tijuana Mexico

PERLA TL Lateral Connector (SpineArt) – Labeling Error (2021)

Due to external labelling error/mix-up. Affected product external labels list the incorrect rod size.

FDAApr 9, 2021Nationwide• SPINEART SA Chemin Du Pre-Fleuri 3 Plan-Les-Ouates Switzerland

Stargate Dump Trailer (Stargate) – Steering Fastener Issue (2021)

Stargate Manufacturing Ltd (Stargate) is recalling certain 2018-2019 DUMP trailers equipped with the Smart-Steer 2.0 self-steering axle with a bolt-on steer arm at 8-7/8" tie-rod location. Under heavy loading, the bolts attaching the steer arm to the knuckle can shear.

NHTSAApr 5, 2021Nationwide• STARGATE

GORE VIBIL Biliary Endoprosthesis (W.L. Gore) – Length Discrepancy (2021)

The Gore post market surveillance team received a complaint that a GORE VIABIL Biliary Endoprosthesis appeared shorter than the labeled length.

FDAApr 5, 2021Nationwide• W.L. Gore & Associates, Inc.

Omnia Soft Tissue Punch (Omnia) – Sterilization Concern (2021)

Omnia SRL received a notification from the contract manufacturer informing them of inadequate sterilization processes which have been taking place at their contracted sterilizing facility since 2016.

FDAMar 30, 2021AK, CA, IL +5 more• Omnia SRL Via Fratelli Cairoli 5 Fidenza Italy

Whole Foods Market Cooked Shrimp (Avanti) – Packaging Error (2021)

One lot of uncooked shrimp was inadvertently packaged as cooked shrimp.

Class IIILow

FDAMar 20, 2021Nationwide• Avanti Frozen Foods Private Limited

Omeprazole Capsules (Golden State) – Impurity Concern (2021)

Failed Impurities/Degradation Specifications: Out of Specification results obtained for unknown impurities during stability testing by manufacturer

Class IIModerate

FDAMar 19, 2021IN, PA, TX• Golden State Medical Supply Inc.

Real Alkalized Water (Real Water) – liver failure (2021)

Laceration Risk

FDA was notified of cases of acute liver failure after consumption of Real Water

Class IHigh

FDAMar 17, 2021Nationwide• Real Water, Inc.

Real Alkalized Water Concentrate (Real Water) – liver failure (2021)

Laceration Risk

FDA was notified of cases of acute liver failure after consumption of Real Water

Class IHigh

FDAMar 17, 2021Nationwide• Real Water, Inc.

Coffee Toffee Chocolate Bar (Mindo) – undeclared milk (2021)

Undeclared Milk

Undeclared milk

Class IIModerate

FDAMar 11, 2021IN, MI• Mindo Chocolate Makers LLC

CyberKnife Treatment System (Accuray) – Couch Roll Risk (2021)

The set screws that connect the Standard Treatment Couch linkage arm to the roll motor can loosen over time allowing the couch to roll.

FDAFeb 26, 2021Nationwide• Accuray Incorporated

MedSchenker STM System (Vectornate) – Culture Media Discoloration (2021)

Discoloration and turbidity were present in the specified lots of STMs because of Longer Monsoon season at the South Korean Manufacturing Facility.

FDAFeb 16, 2021Nationwide• Vectornate USA Inc

Vertical Drain Tube Device (Hollister) – Tube Holder Separation (2021)

The tube holder can separate from the barrier that secures the device to the patients' body. The tube holder has the potential failure to separate from the barrier. This separation might contribute to the potential risk of the tube/drain/catheter migration or loss.

FDAFeb 11, 2021Nationwide• Hollister Incorporated

Thread-Like Wire Marker (Somatex) – Wire Splintering Risk (2021)

This recall has been initiated due to the risk of wire splintering after contact with a cautery device during the removal of a lesion. There is a potential risk that wire fragments are not removed during the procedure and stays inside the patient's body.

FDAFeb 3, 2021MO, NJ, OH• Somatex Medical Technologies GMBH Hohenzollerndamm 150-151 Berlin Germany

ConMed Abdominal Insufflator (Northgate) – Tubing Material Issue (2021)

An internal tubing component in the flow path was made with incorrect material which was not tested for use with this device.

FDAJan 15, 2021Nationwide• Northgate Technologies, Inc.

Steris CO2 Insufflator (Northgate) – Tubing Material Issue (2021)

An internal tubing component in the flow path was made with incorrect material which was not tested for use with this device.

FDAJan 15, 2021Nationwide• Northgate Technologies, Inc.