Product may have low levels of imidacloprid in excess of the tolerance of 0.05 ppm.
All Recalls
95,025 total recalls in our database
The firm received positive test results for Listeria monocytogenes during in house environmental sampling on one of their meat slicers.
Vitamin D3 stability sample analyzed and found to be less than 100% of label claim.
Ingredient containing mold was used in production
FRESH TO YOU Turkey & Sundried Tomato Mayo Pita, Net Wt. 8.29oz (235g), MG Foods Charlotte, NC 28208, UPC MGF9806
Canteen Inc.
The firm received positive test results for Listeria monocytogenes during in house environmental sampling on one of their meat slicers.
Failed Moisture Limits: Out of specification for water content
Sp-4, 100 mL solution bottles, Rx only, Washington Homeopathic Products, Inc.260 J R Hawvermale Way Berkeley Springs West Virginia 25411
Washington Homeopathic Products
An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.
Ganirelix Acetate Injection, 250 mcg/0.5 mL, Sterile Prefilled Syringe, Rx only, Distributor: Ferring Pharmaceuticals, Inc., Parsippany, NJ 07054 USA, Manufactured by: Sun Pharmaceutical Industries Ltd, Halol, Gujarat, India Made in India, NDC 55566-1000-1.
SUN PHARMACEUTICAL INDUSTRIES
Failed Impurities/Degradation Specifications
LCL-2-0191, 5 gallon carboys, Rx only, Manufactured for: LaCore Labs, LLC, by: Washington Homeopathic Products, Inc.260 J R Hawvermale Way Berkeley Springs West Virginia 25411
Washington Homeopathic Products
An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.
Mometasone Furoate Topical Solution, USP, 0.1%, (Lotion), a) 30 mL (NDC 0713-0701-85) and b) 60 mL (NDC 0713-0701-53), Rx Only, Distributed by: Cosette Pharmaceuticals, Inc., South Plainfield, NJ 07080
Cosette Pharmaceuticals
CGMP Deviaitons
Neomycin Sulfate Tablets, USP 500mg, Rx Only, 10x10 Unit dose 100 Tablets, Manufactured for: X-GEN Phamaceuticals, Inc. Big Flats, NY 14814. NDC 39822-0310-5
X-Gen Pharmaceuticals
Failed Stability Specifications: Out of Specification (OOS) result reported for microbiological assay
Telmisartan Tablets, USP 20 mg, 30-count bottles, Rx only, Manufactured by: Alembic Pharmaceuticals Limited (Formulation Division) Panelav 38935, Gujarat, India Manufactured for: Alembic Pharmaceuticals, Inc. 750 Route 202, Bridgewater, NJ 08807, NDC 62332-087-30
Alembic Pharmaceuticals Limited
Labeling: Label-mixup
Macula Pellets Homeopathic Medicine, 1 Oz bottles, Rx only, Manufactured for: Natural Ophthalmics Inc. PO Box 1510 Dillon, CO 80435, NDC 58770-190-42
Washington Homeopathic Products
An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.
Labeling; Label Mix-up; some bottles containing Foam Skin Cleanser soap are incorrectly labeled as Moisturizing Foam Hand Sanitizer
Cross Contamination with Other Product: Product is being recalled due to Trace Amounts of Quetiapine Fumarate
SHARP MEDICAL PRODUCTS, LLC Reactor and Sleeve REF 100-36-01 Size: Adult
Sharp Medical Products
Non-conformity (holes/punctures or deep creases) in the sterile barrier.
At Home Semi-Flex/Rigid Insemination Device (SKU 644042787903)
Tenderneeds Fertility
Device was distributed without a proper marketing authorization.
There is the potential for the Controller power cables (AC Adapter, DC Adapter, and Battery cables), HVAD Alarm Adapter, and HVAD Monitor data cables to cause damage to the HVAD Controller ports when inserting the cables into the Controller ports, due to wear from misalignment of the cables to the port.
MicroScan WalkAway-40 plus Instrument
Beckman Coulter
Instruments were manufactured with a shortened 30mL reagent draw straw which may result in reagents not dispensing and may lead to organism misidentification and/or Quality Control (QC) failure.
MicroScan WalkAway-40 plus Reconditioned Instrument
Beckman Coulter
Instruments were manufactured with a shortened 30mL reagent draw straw which may result in reagents not dispensing and may lead to organism misidentification and/or Quality Control (QC) failure.