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THE KRAFT HEINZ COMPANY

THE KRAFT HEINZ COMPANY Recalls

All product recalls associated with THE KRAFT HEINZ COMPANY.

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Recall Summary

Total Recalls

398

Past Year

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 221–240 of 398 recalls

Breakstones Small Curd Cottage Cheese (Kraft Heinz) – plastic/metal pieces (2019)

Potential presence of pieces of red plastic and metal that may have been introduced during production.

Class IIModerate

FDANov 15, 2019Nationwide• THE KRAFT HEINZ COMPANY

2020 KZRV CONNECT Recall: EQUIPMENT:MECHANICAL:CARRIER/RACK

KZRV, L.P. (KZRV) is recalling certain 2019-2020 Connect and Sportsmen trailers equipped with an optional Rock Run flip up rear storage rack. The racks may detach from the trailer when loaded.

NHTSANov 5, 2019Nationwide• KZRV

Karl Storz Endoscopy: Karl Storz, Model # 11161C2, Flexible Neuroscope

During a complaint investigation it was determined that an error was observed within the instruction manual included with some scopes. Specifically, The Quick Connector Kits (QCK) and tray information, specified for the STERIS System 1E (SS1E) sterilization method within the instruction manual is incorrect. If the user uses SS1E to sterilize the impacted scopes and referred to the manual concerning the QCK information, the sterility of reprocessed scope cannot be guaranteed.

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FDAAug 27, 2019AL, AZ, CA +25 more• Karl Storz Endoscopy

Karl Storz Endoscopy: Karl Storz RHINO-LARYNGO-BRONCHO FIBERSCOPE, Model # 110...

FDAAug 27, 2019AL, AZ, CA +25 more• Karl Storz Endoscopy

Karl Storz Endoscopy: Karl Storz NEURO-FIBERSCOPE, Model # 11282BN1, Flexible P...

FDAAug 27, 2019AL, AZ, CA +25 more• Karl Storz Endoscopy

ARJOHUNTLEIGH POLSKA Sp. z.o.o. Ui. Ks. Piotra Wawrzyniaka 2 Komorniki Poland: Concerto & Basic Shower Trolly, Model Numbers BAB1000-01...

The firm has become aware that any of the 4 safety catches may exhibit a mechanical failure (break in one of the arms of safety catch), which in certain circumstances may contribute to the side support unintentionally opening and may lead to a potential risk of a patient fall. The patient falling could lead to various types of injuries.

FDAAug 22, 2019CA, CO, CT +12 more• ARJOHUNTLEIGH POLSKA Sp. z.o.o. Ui. Ks. Piotra Wawrzyniaka 2 Komorniki Poland

Thoratec Switzerland GMBH Technoparkstrasse 1 Zurich Switzerland: CentriMag Acute Circulatory Support System Motor, U.S. Mo...

Reports have been received of the CentriMag Systems experiencing motor and pump issues resulting from electromagnetic interference (EMI).

FDAAug 22, 2019Nationwide• Thoratec Switzerland GMBH Technoparkstrasse 1 Zurich Switzerland

Enztec Limited 26 Dakota Crescent, Sockburn Christchurch New Zealand: REF 800-05-035, ENZTEC FEMORAL IMPACTOR - DJO, (01) 09421...

The femoral impactors have a higher than normal risk of the arm breaking. During impaction the tip of the arm may fracture and separate from the instrument. This may cause a minor delay in surgery. If not retrieved, it may cause an inflammatory response that may require revision surgery.

FDAAug 16, 2019CA• Enztec Limited 26 Dakota Crescent, Sockburn Christchurch New Zealand