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DILIP CERAMICS DBA SHIVAM DISTRIBUT

DILIP CERAMICS DBA SHIVAM DISTRIBUT Recalls

All product recalls associated with DILIP CERAMICS DBA SHIVAM DISTRIBUT.

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Recall Summary

Total Recalls

1000

Past Year

579

Class I (Serious)

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 4361–4380 of 10937 recalls

Parivar Dry Dates (Dilip Ceramics) – High Sulfites (2019)

Product contains high levels of sulfites (114.65 mg/serving)

Class IHigh

FDAOct 23, 2019FL, IN• DILIP CERAMICS DBA SHIVAM DISTRIBUT

Regular Strength Acid Reducer (Perrigo) – NDMA Contamination (2019)

CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

Class IIModerate

FDAOct 23, 2019Nationwide• Perrigo Company PLC

Acid Reducer Tablets (Perrigo) – NDMA Contamination (2019)

CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

Class IIModerate

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FDA

Oct 23, 2019

Nationwide

• Perrigo Company PLC

Regular Strength Acid Reducer (Perrigo) – NDMA Contamination (2019)

CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

Class IIModerate

FDAOct 23, 2019Nationwide• Perrigo Company PLC

Acid Reducer Ranitidine (Perrigo) – potential contamination (2019)

CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

Class IIModerate

FDAOct 23, 2019Nationwide• Perrigo Company PLC

Acid Reducer Tablets (Perrigo) – NDMA Contamination (2019)

CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

Class IIModerate

FDAOct 23, 2019Nationwide• Perrigo Company PLC

Acid Reducer Cool Mint (Perrigo) – NDMA Contamination (2019)

CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

Class IIModerate

FDAOct 23, 2019Nationwide• Perrigo Company PLC

Acid Reducer Ranitidine (Perrigo) – potential contamination (2019)

CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

Class IIModerate

FDAOct 23, 2019Nationwide• Perrigo Company PLC

Blackhawk T-Series Gun Holsters (Federal Cartridge) – Injury Risk (2019)

Fire/Burn Risk

This recall involves the Blackhawk T-Series black gun holster L2C made of molded plastic material. The black holster is designed to be used with Sig Sauer P320/P250 civilian firearms that clip onto the user's belt. "2101213 A" is printed on the outside of the recalled gun holsters.

High

CPSCOct 22, 2019Nationwide• Federal Cartridge Company, of Manhattan, Mont. d/b/a Blackhawk, Virginia Beach, Va.

PF-Succinylcholine Chloride (Nephron) – Incorrect Labeling (2019)

Incorrect labeling: Incorrect or missing lot and/or exp date

Class IIILow

FDAOct 21, 2019Nationwide• Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Niti-S Esophageal Stent (Taewoong) – Instruction Manual Error (2019)

Misprinted IFUs shipped with esophageal stents

Low

FDAOct 18, 2019IN• Taewoong Medical Co., Ltd. 14 Gojeong-ro, Wolgot-Myeon, Gimpo-Si, Gyeonggi-Do Korea (the Republic of)

Smooth & Creamy Take the Cake Ice Cream (Harris Teeter) – undeclared soy (2019)

The firm discovered that the allergen soy was not declared in the ingredient statement or allergen declaration.

Class IIModerate

FDAOct 17, 2019AL, NC, VA• Harris Teeter Supermarkets, LLC dba Hunter Farms

Harris Teeter Chocolate Ice Cream – Undeclared Soy (2019)

The firm discovered that the allergen soy was not declared in the ingredient statement or allergen declaration.

Class IIModerate

FDAOct 17, 2019AL, NC, VA• Harris Teeter Supermarkets, LLC dba Hunter Farms

Fresh Market Mint Chip Ice Cream (Harris Teeter) – undeclared soy (2019)

The firm discovered that the allergen soy was not declared in the ingredient statement or allergen declaration.

Class IIModerate

FDAOct 17, 2019AL, NC, VA• Harris Teeter Supermarkets, LLC dba Hunter Farms

Mint Chocolate Chip Ice Cream (Harris Teeter) – undeclared soy (2019)

The firm discovered that the allergen soy was not declared in the ingredient statement or allergen declaration.

Class IIModerate

FDAOct 17, 2019AL, NC, VA• Harris Teeter Supermarkets, LLC dba Hunter Farms

Scenaria CT System (Hitachi) – Cable Attachment Risk (2019)

There is a possibility that the cables to the controller unit may not be affixed properly, creating the potential for a cable to detach during scanning and eject from the system.

Moderate

FDAOct 16, 2019CA, FL, GA +13 more• Hitachi Medical Systems America Inc

Posiflush Saline Syringes (Becton Dickinson) – Labeling Mixup (2019)

Limited number of syringes labeled Posiflush Experimental Product and Not for Human Use being mixed with standard BD Posiflush Pre-Filled Normal Saline Syringes.

Moderate

FDAOct 14, 2019Nationwide• Becton Dickinson & Company

Natural Grocers Organic Soybeans (Natural Grocers) – mold potential (2019)

Firm is recalling two lots of 2 lb. organic soybeans because they have the potential to contain mold.

Class IIILow

FDAOct 14, 2019Nationwide• Vitamin Cottage Natural Foods Market, Inc DBA Natural Grocers

Synchromed II Programmable Pump (Medtronic) – motor gear rotation (2019)

There is a potential for the presence of a foreign particle inside the pump motor assembly which could interfere with the motor gear rotation and lead to a permanent motor stall.

High

FDAOct 11, 2019Nationwide• Medtronic Neuromodulation

Legacy 3 Implant (Implant Direct) – incorrect cover screw (2019)

Through a customer complaint and and internal investigation it was determined that some implant packages contain the incorrect cover screw and extender. This could result in delay in surgery and/or a potential new surgical procedures to place the correct parts. The level of severity varies based on a one or two stage surgery.

Moderate

FDAOct 11, 2019AZ, AR, CA +20 more• Implant Direct Sybron Manufacturing LLC