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Jia You Plastics, of China

Jia You Plastics, of China Recalls

All product recalls associated with Jia You Plastics, of China.

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Recall Summary

Total Recalls

1000

Past Year

303

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 2361–2380 of 4747 recalls

Snowboard Boots (Burton) – Fall Hazard (2018)

This recall involves Step On snowboard boots from the winter 2017-2019 seasons. The recalled boots were sold in a variety of colors. The model name is printed on the inside of the boot tongue. Season Model Name Color Winter 17-18 Sales Sample PHOTON STEP-ON BOOT BLACK Winter 17-18 Sales Sample PHOTON STEP-ON BOOT BLUE PRINT Winter 17-18 Sales Sample FELIX STEP-ON BOOT BLACK Winter 17-18 Sales Sample FELIX STEP-ON BOOT STATIC Winter 17-18 Sales Sample RULER STEP-ON BOOT BLACK Winter 17-18 Sales Sample RULER STEP-ON BOOT GREY TIE DYE Winter 17-18 Sales Sample RULER STEP-ON BOOT TAN Winter 17-18 Sales Sample LIMELIGHT STEP-ON BOOT BLACK Winter 17-18 Sales Sample LIMELIGHT STEP-ON BOOT BLACK/MULTI Winter 17-18 Sales Sample LIMELIGHT STEP-ON BOOT TAN Winter 17-18 Production PHOTON STEP ON BOOT BLACK Winter 17-18 Production PHOTON STEP ON BOOT BLUE PRINT Winter 17-18 Production FELIX STEP ON BOOT BLACK Winter 17-18 Production FELIX STEP ON BOOT STATIC Winter 17-18 Production RULER STEP ON BOOT BLACK Winter 17-18 Production RULER STEP ON BOOT GREY TIE DYE Winter 17-18 Production LIMELIGHT STEP ON BOOT BLACK Winter 17-18 Production LIMELIGHT STEP ON BOOT BLACK/MULTI Winter 18-19 Sales Sample PHOTON STEP ON BOOT CLOVER Winter 18-19 Sales Sample PHOTON STEP ON BOOT BLACK Winter 18-19 Sales Sample FELIX STEP ON BOOT BLACK Winter 18-19 Sales Sample RULER STEP ON BOOT BLACK Winter 18-19 Sales Sample RULER STEP ON BOOT BLACK/CAMO Winter 18-19 Sales Sample LIMELIGHT STEP ON BOOT BLACK Winter 18-19 Sales Sample LIMELIGHT STEP ON BOOT MIDNITE BLOOM Winter 18-19 Sales Sample ION STEP ON BOOT BLACK Winter 18-19 Sales Sample ZIPLINE STEP ON BOOT BLACK Winter 18-19 Sales Sample PHOTON STEP ON - ASIAN FIT BOOT CLOVER Winter 18-19 Sales Sample PHOTON STEP ON - ASIAN FIT BOOT BLACK

CPSCJul 11, 2018Nationwide• Jia You Plastics, of China

Diazepam Rectal Gel (Valeant) – Incorrect Labeling (2018)

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Labeling: Incorrect or Missing Lot and/or Exp Date: Product distributed without a lot number or expiration date on the outer carton.

Class IIILow

FDAJul 10, 2018Nationwide• Valeant Pharmaceuticals North America LLC

Triamterene and Hydrochlorothiazide (Mylan) – Subpotent Drug (2018)

Subpotent Drug

Class IIILow

FDAJul 9, 2018Nationwide• Mylan Pharmaceuticals Inc.

Fluocinolone Acetonide Solution (Teva) – Impurity Issues (2018)

Failed Impurities and Degradation Specifications and Subpotent Drug: out-of-specification (OOS) test results for below assay and above specification for degradants.

Class IIModerate

FDAJul 5, 2018Nationwide• Teva Pharmaceuticals USA

Metformin Extended Release (Sun Pharmaceutical) – Foreign Substance (2018)

Presence of foreign substance: One lot fo Metformin Hydrochloride Extended Release Tablets, USP, 500 mg (500 Count) contains foreign matter identified as a piece of rubber glove detected in one tablet.

Class IIModerate

FDAJul 3, 2018AZ• Sun Pharmaceutical Industries, Inc.

Buffered Lidocaine Injection (SCA Pharmaceuticals) – subpotent drug (2018)

Subpotent Drug: Stability data does not support the current expiration dating of 55 days after compounding.

Class IIModerate

FDAJun 29, 2018Nationwide• SCA Pharmaceuticals

Prescript-Assist Probiotic (LL's Magnetic Clay) – Undeclared Allergens (2018)

Undeclared Allergen

The recalled dietary supplement has the potential to contain undeclared allergens, including almonds, shellfish, milk, eggs, and peanuts.

Class IHigh

FDAJun 29, 2018Nationwide• LL'S MAGNETIC CLAY INC

Enalapril Maleate 5mg (Aidarex) – degradation product (2018)

Out-of-specification results for the Enalapril Diketopiperazine degradation product during commercial stability.

Class IIILow

FDAJun 27, 2018Nationwide• Aidarex Pharmaceuticals LLC

Enalapril Maleate 5mg 90-count (Aidarex) – degradation product (2018)

Out-of-specification results for the Enalapril Diketopiperazine degradation product during commercial stability.

Class IIILow

FDAJun 27, 2018Nationwide• Aidarex Pharmaceuticals LLC

Enalapril Maleate 2.5mg (Aidarex) – degradation product (2018)

Out-of-specification results for the Enalapril Diketopiperazine degradation product during commercial stability.

Class IIILow

FDAJun 27, 2018Nationwide• Aidarex Pharmaceuticals LLC

Enalapril Maleate 2.5mg Tablets (Major Pharmaceuticals) – impurity specifications (2018)

Failed Impurities/Degradation Specifications: Sub-recall because this repackaged product was recalled by the manufacturing firm, Wockhardt, due to out-of-specification results for the Enalapril DiKetopiperazine degradation product.

Class IIILow

FDAJun 26, 2018Nationwide• MAJOR PHARMACEUTICALS

Enalapril Maleate 5mg Tablets (Major Pharmaceuticals) – impurity specifications (2018)

Class IIILow

FDAJun 26, 2018Nationwide• MAJOR PHARMACEUTICALS

Calcitriol Oral Solution (Validus) – Subpotency Issue (2018)

Subpotency: lower than expected potency result was obtained at the 18 month stability time point.

Class IIILow

FDAJun 15, 2018Nationwide• Validus Pharmaceuticals, Inc.

Rocaltrol Oral Solution (Validus) – Subpotency Issue (2018)

Subpotency: lower than expected potency result was obtained at the 18 month stability time point.

Class IIILow

FDAJun 15, 2018Nationwide• Validus Pharmaceuticals, Inc.