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Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Mylan Institutional, Inc. (d.b.a. UDL Laboratories) Recalls

All product recalls associated with Mylan Institutional, Inc. (d.b.a. UDL Laboratories).

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Recall Summary

Total Recalls

1000

Past Year

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 1441–1460 of 2670 recalls

Loxapine Capsules 50mg (Mylan) – Manufacturing Risk (2018)

GMP Deviations: a recent FDA inspection of the manufacturing site revealed multiple cGMP violations that would place Loxapine at risk for cross contamination

Class IIModerate

FDAMay 1, 2018Nationwide• Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Loxapine Capsules 25mg (Mylan) – Manufacturing Risk (2018)

GMP Deviations: a recent FDA inspection of the manufacturing site revealed multiple cGMP violations that would place Loxapine at risk for cross contamination

Class IIModerate

FDAMay 1, 2018Nationwide• Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Metoprolol Tablets (Dr. Reddy's) – Foreign Tablet Found (2018)

Presence of Foreign Tablets/Capsules: One foreign tablet identified as Clopidogrel 75 mg was found in a 100 count bottle of Metoprolol Succiante Extended-Release Tablets.

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Class IIModerate

FDAApr 23, 2018Nationwide• Dr. Reddy's Laboratories, Inc.

Phoenix 200 ATV (Polaris) – crash hazard (2018)

This recall involves all model year 2014 through 2017 Phoenix 200 all-terrain vehicles. "Polaris" is stamped on the front grill and on the sides of the ATV seats, and "Phoenix 200" is stamped on the side panels. The ATVs were sold in blue and gray. Model numbers A14PB20AF, A15YAP20AF, A16YAP20AF and A17YAP20A8 are included in this recall. The model number is located on the vehicle frame. To check for recalled vehicles by vehicle identification number (VIN) visit www.polaris.com.

CPSCApr 19, 2018Nationwide• Aeon Motor Co., of Taiwan

Fluocinolone Acetonide Ear Drops (Lyne Labs) – Subpotent Drug (2018)

Subpotent Drug

Class IIModerate

FDAApr 13, 2018Nationwide• Lyne Laboratories, Inc.

Fluocinolone Acetonide Body Oil (Lyne Labs) – Subpotent Drug (2018)

Subpotent Drug

Class IIModerate

FDAApr 13, 2018Nationwide• Lyne Laboratories, Inc.

Fluocinolone Acetonide Topical Oil (Lyne Labs) – Subpotent Drug (2018)

Subpotent Drug

Class IIModerate

FDAApr 13, 2018Nationwide• Lyne Laboratories, Inc.

Hunting Knife (Nextorch) – Laceration Hazard (2018)

Laceration Risk

This recall involves the Allagash fixed blade hunting knife with sheath. The sheath measures 7 inches long by 2 inches wide, is made of brown leather and contains white stitching down one side. The knife blade measures 3.55 inches long by 1 inch wide, is made of stainless steel and is attached to a light brown handle. L.L.Bean is embossed on the brown leather sheath and engraved on the top of the knife blade near handle on one side. The recalled knife with sheath has the product identification number 501794 printed on the green box in which the knife is packaged.

CPSCApr 12, 2018Nationwide• Nextorch Industries Co. LTD, of China

Traction Elevators (Residential Elevators) – Impact Hazard (2018)

This recall involves traction residential elevators with models LLT-952, LLT-953, LLT-954 and LLT-955 shipped and installed between January 2015 and April 2017. The recalled elevators are used in consumers' homes. "Residential Elevators" is printed on a label on the operating panel inside the elevator cab.

CPSCMar 29, 2018Nationwide• Residential Elevators Inc., of Crawfordville, Fla.

Pistachio Gelato (Raley's) – unauthorized color additive (2018)

Firm was notified by manufacturer in Italy that Pistachio Gelato contained the color sodium copper chlorophyllins (SCC), which is not authorized by FDA as a color additive for this product type.

Class IIILow

FDAMar 15, 2018CA, NV• Raley's Family of Fine Stores

Clocortolone Pivalate Cream (Dr. Reddy's) – Viscosity Failure (2018)

Failed Stability Specifications:Out-of-specification results observed for viscosity during stability testing.

Class IIILow

FDAMar 8, 2018Nationwide• Dr. Reddy's Laboratories, Inc.

InSinkErator SinkTop Switch (Tecmark) – Fire Hazard (2018)

Fire/Burn Risk

This recall involves InSinkErator Single Outlet SinkTop Switches. The air activated switch mounts to the sink or countertop and is an alternative to the traditional wall switch for a garbage disposal. The model numbers are 76703, STS-SOSN, 78251 and 74300, and can be found on the back of the power module. InSinkErator is written on the front of the power module. The switches were sold with a chrome, white, or satin nickel button/bezel as an accessory for garbage disposals. Garbage disposals activated by a wall switch are not affected by this recall.

CPSCMar 6, 2018Nationwide• Tecmark of Mentor, Ohio

Hydrocodone Bitartrate and Homatropine (Novel) – Impurity Specification (2018)

Failed Impurities/Degradation Specifications

Class IIILow

FDAMar 5, 2018Nationwide• Novel Laboratories, Inc.

Evamist (Paddock) – Defective Delivery System (2018)

Defective Delivery System: Potential that cracks in the vial neck near the crimp may result in product evaporation and/or leaking and the inability to properly dispense product.

Class IIModerate

FDAFeb 26, 2018Nationwide• Paddock Laboratories, LLC.

Thyroid Resilience Supplement (Progressive) – Undeclared Milk (2018)

Undeclared Milk

Recalled dietary supplements may contain undeclared milk.

Class IHigh

FDAFeb 23, 2018Nationwide• Progressive Laboratories, Inc

Xenesta Nuvive Womens Supplement (Progressive) – Undeclared Milk (2018)

Undeclared Milk

Recalled dietary supplements may contain undeclared milk.

Class IHigh

FDAFeb 23, 2018Nationwide• Progressive Laboratories, Inc

Xenesta Nuvive Mens Supplement (Progressive) – Undeclared Milk (2018)

Undeclared Milk

Recalled dietary supplements may contain undeclared milk.

Class IHigh

FDAFeb 23, 2018Nationwide• Progressive Laboratories, Inc

Testosterzone Supplement (Progressive) – Undeclared Milk (2018)

Undeclared Milk

Recalled dietary supplements may contain undeclared milk.

Class IHigh

FDAFeb 23, 2018Nationwide• Progressive Laboratories, Inc

Yamaha Golf Cars and PTVs (Yamaha) – crash hazard (2018)

This recall involves the following model year 2015 through 2018 gas and electric-powered golf cars , PTVs and utility vehicles. The vehicles were sold in various colors including blue, green, red, white, tan and silver. The model and serial numbers can be found on a label under the seat on the left or right side. Model Name Model Year Model Number Serial Number Range The DRIVE Models YDRA (Gas) 2015 JC0 0600101-0606900 JC2 0200101-0211800 JW8 0500101-0516400 2016 JC0 0700101-0706598 JC2 0300101-0312000 JW8 0600101-0614300 The DRIVE Models YDRE (Electric) 2015 JC1 0600101-0603300 JW9 0500101-0518300 2016 JC1 0700101-0703500 JC3 0000101-0004700 JW9 0600101-0618100 The DRIVE 2 Models DR2A (Gas) 2017 J0A 0000101-0010100 J0B 0000101-0016900 J0D 0000101-0007200 2018 J0A 0100101-0105300 J0B 0100101-0107287 J0D 0100101-0104700 The DRIVE 2 Models DR2E (Electric) 2017 J0C 0000101-0011400 J0E 0000101-0002900 J0J 0000101-0001999 2018 J0C 0100101-0105482 J0E 0100101-0101300 J0J 0100101-0100798

CPSCFeb 22, 2018Nationwide• Yamaha Motor Manufacturing Corporation of America, of Newnan, Ga.

2011 VACTOR HXX Recall: EQUIPMENT

Vactor Manufacturing (Vactor) is recalling certain 2011-2017 HXX and 2100 Plus vacuum excavator trucks. The hydraulic dump body cylinder can corrode at the threaded joint over time, causing the cylinder to fail when in a dump cycle.

NHTSAFeb 22, 2018Nationwide• VACTOR