Skip to main content

Is My Product Recalled?

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Scan How It Works Saved Get Alerts

Menu

Search All Recalls Latest Recalls Scan Barcode Get Alerts

Categories

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Resources

How Recalls Work FAQ Recall Classifications Statistics & Trends About

Your Recalls

Loading...

Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

Home
/
Brands
/
Mylan Laboratories Limited, (Nashik FDF)

Mylan Laboratories Limited, (Nashik FDF) Recalls

All product recalls associated with Mylan Laboratories Limited, (Nashik FDF).

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

566

Class I (Serious)

25

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 4141–4160 of 7756 recalls

Amlodipine & Valsartan (Mylan) – NDEA Contamination (2018)

GCMP Deviations: FDA analysis confirmed presence of trace amounts of an impurity, N-nitrosodiethylamine (NDEA) found in the API used to manufacture the product.

Class IIModerate

FDADec 4, 2018Nationwide• Mylan Laboratories Limited, (Nashik FDF)

Valsartan (Mylan) – NDEA Contamination (2018)

GCMP Deviations: FDA analysis confirmed presence of trace amounts of an impurity, N-nitrosodiethylamine (NDEA) found in the API used to manufacture the product.

Class IIModerate

FDADec 4, 2018Nationwide• Mylan Laboratories Limited, (Nashik FDF)

Amlodipine & Valsartan (Mylan) – NDEA Contamination (2018)

GCMP Deviations: FDA analysis confirmed presence of trace amounts of an impurity, N-nitrosodiethylamine (NDEA) found in the API used to manufacture the product.

1...206 207208209 210...388

Page 208 of 388Next

Class IIModerate

FDADec 4, 2018Nationwide• Mylan Laboratories Limited, (Nashik FDF)

Valsartan (Mylan) – NDEA Contamination (2018)

GCMP Deviations: FDA analysis confirmed presence of trace amounts of an impurity, N-nitrosodiethylamine (NDEA) found in the API used to manufacture the product.

Class IIModerate

FDADec 4, 2018Nationwide• Mylan Laboratories Limited, (Nashik FDF)

Amlodipine & Valsartan (Mylan) – NDEA Contamination (2018)

GCMP Deviations: FDA analysis confirmed presence of trace amounts of an impurity, N-nitrosodiethylamine (NDEA) found in the API used to manufacture the product.

Class IIModerate

FDADec 4, 2018Nationwide• Mylan Laboratories Limited, (Nashik FDF)

5-Gallon Mixing Buckets (Lumber Liquidators) – Drowning Hazard (2018)

This recall involves a 5-gallon yellow plastic mixing bucket with LL Pro+ and Lumber Liquidators printed on the outside of the buckets. The buckets have the SKU #10043866 printed on the product label.

CPSCNov 27, 2018Nationwide• Zhejiang Focus-On Import & Export, of Binjiang District, China

Peach Dices (Titan Farms) – foreign material (2018)

Foreign material (plastic)

Class IIModerate

FDANov 21, 2018CA, IN, TN• Titan Farms, Inc. d/b/a Palmetto Processing Solutions

2018 WABASH NATIONAL VAN Recall: STRUCTURE:BODY

Wabash National Corporation (Wabash) is recalling certain 2014-2019 Wabash National Van trailers equipped with limb deflectors. The limb deflectors installed on the upper rear corner of the trailers may detach while moving.

NHTSANov 15, 2018Nationwide• WABASH NATIONAL

Turkey Hill Vanilla Ice Cream (Hunter Farms) – Mislabeled Ingredients (2018)

Package did not contain Vanilla Bean Ice Cream but Cotton Candy Ice Cream, which contains soy lecithin that is not listed on the Vanilla Bean label.

Class IIModerate

FDANov 15, 2018IN, PA• Harris Teeter Supermarkets, LLC dba Hunter Farms

Quetiapine Tablets (Ascend Labs) – Metal Shard Found (2018)

Presence of Foreign Substance; metal shard found in tablet

Class IIModerate

FDANov 14, 2018Nationwide• Ascend Laboratories LLC

Recchiuti Bittersweet (Recchiuti) – undeclared milk (2018)

FDA analysis of Dairy Free Dark Chocolate found high levels of milk protein in the chocolate bars.

FDANov 9, 2018CA, IN• Confections by Michael Recchiuti

Recchiuti Feve Dark Chocolate (Recchiuti) – undeclared milk (2018)

FDA analysis of Dairy Free Dark Chocolate found high levels of milk protein in the chocolate bars

FDANov 9, 2018CA, IN• Confections by Michael Recchiuti

Girls Clothing Set (Ningbo Younker) – lead content violation (2018)

Laceration Risk

This recall involves Self-Esteem brand girl's clothing sets with a gold leaf pendant necklace. The recalled clothing sets consists of three items: a short-sleeve teal top with cut-out shoulders, a navy blue legging pant with a teal floral print and a pendant necklace with an orange and teal center. The recalled clothing sets have style number PO#71160/LOT9 and a date of production of 10/2017 printed on a white label on the inside of the garment. The recalled clothing sets were sold in girl's sizes 4x-12x.

CPSCNov 8, 2018Nationwide• Ningbo Younker Fashion Accessory Industrial Corporation, of China

Sweet Basil Leaf (Black River Industries) – plastic contamination (2018)

Parsley Flakes are being recalled because they may contain a foreign material (plastic). EXPANDED 1127/2018 During processing it was noted that Basil Leaf Sweet and Italian Spice Blend No Salt also may contain foreign material (plastic).

Class IIModerate

FDANov 8, 2018WI• Black River Industries

Italian Spice Blend (Black River Industries) – plastic contamination (2018)

Parsley Flakes are being recalled because they may contain a foreign material (plastic). EXPANDED 1127/2018 During processing it was noted that Basil Leaf Sweet and Italian Spice Blend No Salt also may contain foreign material (plastic).

Class IIModerate

FDANov 8, 2018WI• Black River Industries

Parsley Flakes (Black River Industries) – plastic contamination (2018)

Parsley Flakes are being recalled because they may contain a foreign material (plastic). EXPANDED 1127/2018 During processing it was noted that Basil Leaf Sweet and Italian Spice Blend No Salt also may contain foreign material (plastic).

Class IIModerate

FDANov 8, 2018WI• Black River Industries

Kubota Mowers and Tractors (Kubota) – burn hazard (2018)

This recall involves model year 2014 to 2018 Kubota with model numbers BX, GR, ZD and ZG, diesel and gasoline-powered zero turn mowers, compact tractors, and ride-on mowers. The model number is printed on the side of the unit. Kubota is printed on the side of the mowers and tractors. The data plate has the serial number and is also located on the side of the unit. Recalled units are orange and black. Model Serial Number Range Production Date BX1870-1 BEGIN END 20323 26954 7/7/2014 8/17/2018 BX1880 BEGIN END 10002 14813 BX23S BEGIN END 10007 25677 BX25D BEGIN END 17263 17269 7/7/2014 8/17/2018 BX25-1 BEGIN END 20002 52688 BX2370-1 BEGIN END 20740 52083 BX2380 BEGIN END 10008 25675 BX2670 BEGIN END 13836 13839 7/7/2014 8/17/2018 BX2670-1 BEGIN END 20370 50557 BX2680 BEGIN END 10004 16435 7/7/2014 8/17/2018 GR2120 BEGIN END 16256 37133 7/7/2014 8/17/2018 ZD1011 BEGIN END 10004 13271 ZD1021-60 BEGIN END 10004 12809 ZD1211-60 BEGIN END 10002 28405 7/7/2014 8/17/2018 ZD1211R-60R BEGIN END 10002 20642 ZD1211L-72 BEGIN END 10002 24621 ZD1211RL-72R BEGIN END 10002 20457 ZD221 BEGIN END 33698 35861 ZD323-60 BEGIN END 35702 37252 ZD326HL-72 BEGIN END 10005 12054 7/7/2014 8/17/2018 ZD326P-60 BEGIN END 39440 44820 ZD326RP-60R BEGIN END 12065 12786 ZD326S-60 BEGIN END 35207 37450 ZD331RP-60R BEGIN END 11015 11131 ZG332LP BEGIN END 10672 10737 7/7/2014 8/17/2018 ZG332P-60 BEGIN END 10688 10694

CPSCNov 7, 2018Nationwide• Kubota Manufacturing of America Corporation, of Gainesville, Ga.

Clopidogrel Tablets (Dr. Reddy's) – Dissolution Failure (2018)

Failed Dissolution Specification: Out-of-Specification results were observed for dissolution at 18th month stability testing.

Class IIModerate

FDANov 7, 2018Nationwide• Dr. Reddy's Laboratories, Inc.

Megestrol Acetate Suspension (Breckenridge) – Stability Issue (2018)

Failed Stability Specifications: Out-of-Specification results obtained for particle size distribution during stability testing.

FDANov 6, 2018Nationwide• Breckenridge Pharmaceutical, Inc.

Numbify Pain Relief (Pain Relief Naturally) – Compliance Failure (2018)

This recall involves all Pain Relief Naturally lidocaine-containing products including Numbify, Extra Strength Numbify, Pre-TAT Tattoo, Superior Pain & Itch Relief, and Soothing Sore Relief creams, sprays, gels and liquid gels. The recalled products were sold in 1, 2 and 4 ounce size containers. The products have black packaging with the name of the product in gold, red, or green lettering. Numbify Cream, Spray, Gel & Liquid Gel Black tubs and bottles with gold lettering Extra Strength Numbify Cream, Spray, Gel & Liquid Gel Black tubs and bottles with gold lettering Pre-TAT Tattoo Cream, Spray, Gel & Liquid Gel Black tubs and bottles with red lettering Superior Pain & Itch Relief Cream, Spray, Gel & Liquid Gel Black tubs and bottles with green lettering Soothing Sore Relief Cream, Spray, Gel & Liquid Gel Black tubs and bottles with green lettering

CPSCNov 1, 2018Nationwide• Ridge Properties, DBA Pain Relief Naturally, of Salem, Ore.