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K & P Marketplace Ltd. d.b.a Mt. Kisco Smokehouse Ltd.

K & P Marketplace Ltd. d.b.a Mt. Kisco Smokehouse Ltd. Recalls

All product recalls associated with K & P Marketplace Ltd. d.b.a Mt. Kisco Smokehouse Ltd..

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Recall Summary

Total Recalls

1000

Past Year

579

Class I (Serious)

91

Most Recent

Dec 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 5901–5920 of 10937 recalls

Sliced Smoked Salmon (Mt. Kisco Smokehouse) – Listeria Contamination (2016)

Environmental samples collected by the Food and Drug Administration revealed the presence of Listeria monocytogenes which has the potential to contaminate food products.

FDASep 26, 2016CT, NY• K & P Marketplace Ltd. d.b.a Mt. Kisco Smokehouse Ltd.

Atlantic Smoked Salmon (Mt. Kisco Smokehouse) – Listeria Contamination (2016)

Environmental samples collected by the Food and Drug Administration revealed the presence of Listeria monocytogenes which has the potential to contaminate food products.

FDASep 26, 2016CT, NY• K & P Marketplace Ltd. d.b.a Mt. Kisco Smokehouse Ltd.

Cyclopentolate HCl 1% - Tropicamide 1% (Leiter's) – sterility risk (2016)

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Lack of Assurance of Sterility; all compounded products within expiry produced using recalled filters

Class IIModerate

FDASep 20, 2016Nationwide• Leiter's Compounding

Mitomycin 0.02% Injection (Leiter's Compounding) – Sterility Concern (2016)

Lack of Assurance of Sterility; all compounded products within expiry produced using recalled filters

Class IIModerate

FDASep 20, 2016Nationwide• Leiter's Compounding

Brilliant Blue G Injection (Leiter's) – sterility risk (2016)

Lack of Assurance of Sterility; all compounded products within expiry produced using recalled filters

Class IIModerate

FDASep 20, 2016Nationwide• Leiter's Compounding

Moxifloxacin Sterile Solution (Leiter's) – sterility risk (2016)

Lack of Assurance of Sterility; all compounded products within expiry produced using recalled filters

Class IIModerate

FDASep 20, 2016Nationwide• Leiter's Compounding

Cefuroxime Sodium Injection (Leiter's) – sterility risk (2016)

Lack of Assurance of Sterility; all compounded products within expiry produced using recalled filters

Class IIModerate

FDASep 20, 2016Nationwide• Leiter's Compounding

Lidocaine HCl Injection (Leiter's) – sterility risk (2016)

Lack of Assurance of Sterility; all compounded products within expiry produced using recalled filters

Class IIModerate

FDASep 20, 2016Nationwide• Leiter's Compounding

Vancomycin Injection (Leiter's) – sterility risk (2016)

Lack of Assurance of Sterility; all compounded products within expiry produced using recalled filters

Class IIModerate

FDASep 20, 2016Nationwide• Leiter's Compounding

Prednisolone Acetate Placebo (Leiter's) – sterility risk (2016)

Lack of Assurance of Sterility; all compounded products within expiry produced using recalled filters

Class IIModerate

FDASep 20, 2016Nationwide• Leiter's Compounding

Atropine Sulfate Solution (Leiter's) – sterility risk (2016)

Lack of Assurance of Sterility; all compounded products within expiry produced using recalled filters

Class IIModerate

FDASep 20, 2016Nationwide• Leiter's Compounding

Marcaine 0.25% Injection (Hospira) – Sterility Risk (2016)

Lack of Assurance of Sterility and Subpotent Drug: defect in glass vial prevented stopper from forming a seal allowing water to ingress and dilute the product causing it to be less than the labeled potency.

Class IIModerate

FDASep 16, 2016Nationwide• Hospira Inc., A Pfizer Company

Marcaine 0.5% Injection (Hospira) – Sterility Risk (2016)

Lack of Assurance of Sterility and Subpotent Drug: defect in glass vial prevented stopper from forming a seal allowing water to ingress and dilute the product causing it to be less than the labeled potency.

Class IIModerate

FDASep 16, 2016Nationwide• Hospira Inc., A Pfizer Company

Galaxy Note7 Smartphone (Samsung) – Fire and burn hazard (2016)

This recall involves the Samsung Galaxy Note7 smartphone sold before September 15, 2016. The recalled devices have a 5.7 inch screen and were sold in the following colors: black onyx, blue coral, gold platinum and silver titanium with a matching stylus. Samsung is printed on the top front of the phone and Galaxy Note7 is printed on the back of the phone. To determine if your phone has been recalled, locate the IMEI number on the back of the phone or the packaging, and enter the IMEI number into the online registration site www.samsung.com or call Samsung toll-free at 844-365-6197.

CPSCSep 15, 2016Nationwide• Samsung Electronics America Inc., of Ridgefield Park, N.J.

Ondansetron HCI API (Cadila) – Microbial Contamination (2016)

Microbial Contamination of Non-Sterile Product

Class IIModerate

FDASep 9, 2016IN• Cadila Pharmaceuticals Limited

Mannish Water Soup (Island Soups) – Botulinum Risk (2016)

Possible contamination with Clostridium botulinum

Class IIModerate

FDASep 7, 2016Nationwide• Island Soups Company Inc.

Gungo Peas Soup No Meat (Island Soups) – Botulinum Risk (2016)

Possible contamination with Clostridium botulinum

Class IIModerate

FDASep 7, 2016Nationwide• Island Soups Company Inc.

Red Peas Soup No Meat (Island Soups) – Botulinum Risk (2016)

Possible contamination with Clostridium botulinum

Class IIModerate

FDASep 7, 2016Nationwide• Island Soups Company Inc.

Whole Wheat Flour (Baker's Scoop) – Nylon Fragment Risk (2016)

Potential for the presence of soft nylon fragments in the whole wheat flour.

FDASep 7, 2016TX• C. H. Guenther & Son, Inc.dba Morrison Milling

Varithena (Biocompatibles) – Incorrect Syringe (2016)

Defective Delivery System: Incorrect type of syringe found in commercially distributed administration pack

FDASep 7, 2016Nationwide• Biocompatibles U.K., Ltd.