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 ↗

RSS Feed

Home
/
Brands
/
Luitpold Pharmaceuticals, Inc.

Luitpold Pharmaceuticals, Inc. Recalls

All product recalls associated with Luitpold Pharmaceuticals, Inc..

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

304

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 4221–4240 of 4747 recalls

Epinephrine Injection (Luitpold) – particulate matter (2012)

Presence of Particulate Matter

Class IIModerate

FDAApr 24, 2012Nationwide• Luitpold Pharmaceuticals, Inc.

Jolessa Tablets (Teva) – contraceptive sequence issue (2012)

Contraceptive Tablets Out of Sequence: This recall has been initiated due to the potential that some regimen packages may not contain placebo tablets.

Class IIILow

FDAApr 23, 2012Nationwide• Teva Pharmaceuticals USA, Inc.

Multihance Injection (Bracco) – Short Fill Potential (2012)

Short Fill: The product is being recalled due to a potential underfill of the affected vials.

Class III

1...210 211212213 214...238

Page 212 of 238Next

Low

FDAApr 16, 2012Nationwide• Bracco Diagnostics Inc

Multihance Injection (Bracco) – Sterility Concern (2012)

Lack of Assurance of Sterility; Product recalled due to displacement of the aluminum crimp cap during product usage.

Class IIModerate

FDAApr 16, 2012Nationwide• Bracco Diagnostics Inc

Fosphenytoin Sodium Injection 500mg (West-ward) – Particulate Matter (2012)

Presence of Particulate Matter: This product is being recalled due to the discovery of particles in the stability samples and retain samples.

Class IIModerate

FDAApr 13, 2012Nationwide• West-ward Pharmaceutical Corp.

Fosphenytoin Sodium Injection 100mg (West-ward) – Particulate Matter (2012)

Presence of Particulate Matter: This product is being recalled due to the discovery of particles in the stability samples and retain samples.

Class IIModerate

FDAApr 13, 2012Nationwide• West-ward Pharmaceutical Corp.

Mefloquine HCL Tablets (Teva) – weight inconsistency (2012)

Tablet Thickness: Product is being recalled due to the potential of being underweight or overweight.

Class IIModerate

FDAApr 2, 2012Nationwide• Teva Pharmaceuticals USA, Inc.

Daytrana Patch (Noven Pharmaceuticals) – Delivery System Defect (2012)

Miscalibrated/Defective Delivery System; exceeded the specification for both mechanical peel force (MPF) and/or the z-statistic value

Class IIModerate

FDAMar 22, 2012Nationwide• Noven Pharmaceuticals, Inc.

Metformin Tablets (Zydus Pharmaceuticals) – Foreign Substance (2012)

Presence of Foreign Substance(s): A product complaint was received from a pharmacist who discovered that several tablets displayed brown specks. The same complainant also reported that metal shaving like material was observed on the surface of one tablet.

Class IIModerate

FDAMar 14, 2012Nationwide• Zydus Pharmaceuticals USA Inc

Ciprofloxacin Tablets (Pack Pharmaceuticals) – missing label (2012)

Labeling Illegible: Missing Label; The voluntary recall of the aforementioned batch of product is being initiated due to two bottles missing container labels.

Class IIILow

FDAMar 9, 2012Nationwide• Pack Pharmaceuticals

Arctic Cat Snowmobiles (Arctic Cat) – Crash Hazard (2012)

The recall involves the 2012 model year of the F, XF, and M model snowmobiles. Model Model Name/Number F F800 LXR, F1100 LXR, F800 Sno Pro, F1100 Turbos, F1100 Sno Pro/Limited/50th XF XF800 LXR, XF1100 LXR, XF800 Sno Pro High Country, XF1100 Turbos, XF100 Limited/50th M M800, M1100, M800 Sno Pro, M1100 Sno Pro/Limited/50th, M800 HCR, M1100 Turbos The model name is located on each side of the hood. The snowmobiles were sold in a variety of these color combinations: black, white and orange, black and orange, black and green and white and green.

CPSCJan 31, 2012Nationwide• Arctic Cat Inc., of Thief River Falls, Minn.

Roundy's Butter Cookies (Atico) – Bacterial Contamination (2012)

Atico International USA, Inc. is recalling Roundy's Rich Fields Butter Cookies due to Toxigenic Bacillus cereus found in a sample tested by FDA.

Class IIModerate

FDAJan 20, 2012WI• Atico International USA, Inc.

Arctic Cat Snowmobiles – crash hazard (2011)

The recall involves the following 2012 F, XF, and M model snowmobiles: Model Model Name/Number F F800 LXR, F1100 LXR, F800 Sno Pro, F1100 Sno Pro/Limited/50th XF XF800 LXR, XF1100 LXR, XF800 Sno Pro High Country, XF1100 Limited/50th M M800, M1100, M800 Sno Pro, M1100 Sno Pro/Limited/50th, M800 HCR Recalled snowmobiles can be identified by the last six numerals of the Vehicle Identification Number (VIN) in the following ranges: 105092 through 112175 or 800001 through 800033. The model name is located on each side of the hood. The VIN is located on the right side tunnel. The snowmobiles come in a variety of color combinations: Black, White and Orange, Black and Orange, and Black and Green.

CPSCDec 15, 2011Nationwide• Arctic Cat Inc., of Thief River Falls, Minn.

Argatroban Injection (Eagle) – Crystalline Particulates (2011)

A complaint was received from a hospital pharmacy on 11/10/11 for crystalline particulates in a single vial from Lot V10194. Additional small visible particles consisting of fibers were identified.

Class IHigh

FDADec 2, 2011NJ• Eagle Pharmaceuticals Inc.

Magnetic Sketchboards (Battat) – Choking Hazard (2011)

Choking Hazard

This recall involves the Toulouse-LapTrec magnetic sketchboard, which has a white plastic writing surface bordered by either a red or brown plastic frame, and has a bean bag type backing. The sketch board has four animal shapes across the top - a rabbit, dog, cat and duck. The multicolored magnetic pen is affixed to the front of the sketchpad. The model number BX1026 (red frame) or BX1027 (brown frame) can be found on a paper wrapper that comes with the product at the time it was purchased.

CPSCNov 2, 2011Nationwide• Rainbow Force Plastic Products, of China

Glider Recliners (Big Lots) – Entrapment Risk (2011)

The Microfiber Glider Recliner and Leather Glider Recliner are reclining glider/rocking chairs on a swivel base. Both the chair and ottoman sit on circular metal bases made from 1.25 inch metal tubing and have cushions covered in either light brown or green microfiber fabric or dark brown simulated leather fabric. A label under the seat of the chair identifies the manufacturer as Dongguan Shindin Metal and Plastic Products Ltd. There is a small label on the front metal rod under the seat that states "Maximum wt load 250 lbs."

CPSCOct 25, 2011Nationwide• Dongguan Shindin Metal & Plastic Products Ltd., of China

Prefera OB One Gel Capsules (Meda) – Undeclared Ingredients (2011)

Undeclared Allergen

Labeling: Presence of Undeclared Color Additive; The product is being recalled because several inactive ingredients were not included in the labeling for this product: Undeclared D&C Red #33, FD&C Blue #1, Titanium Dioxide Suspension, Purified Water USP.

Class IIModerate

FDAOct 17, 2011Nationwide• Meda Pharmaceuticals Inc.

Daytrana 10mg Patch (Noven) - Delivery System Issue (2011)

Miscalibrated and/or Defective Delivery System: Out of Specification results for mechanical peel force and/or the z-statistic value which relates to the patient's ability to remove the release liner from the patch adhesive prior to administration.

Class IIModerate

FDAJul 5, 2011Nationwide• Noven Pharmaceuticals, Inc.

Daytrana Patch (Noven) – Delivery System Defect (2011)

Class IIModerate

FDAJul 5, 2011Nationwide• Noven Pharmaceuticals, Inc.

Daytrana Patch (Noven) - Delivery System Issue (2011)

Class IIModerate

FDAJul 5, 2011Nationwide• Noven Pharmaceuticals, Inc.