Product recalled due to the presence of yellow oleander and its components in the product.
All Recalls
95,083 total recalls in our database
Undeclared allergen milk (whey) and undeclared lard
Brazil Seed Net WT 0.18 oz (5g)
HandNatural
Product recalled due to the presence of yellow oleander and its components in the product.
Label mix-up product is labeled as black peppercorn but is actually Pink Himalayan salt
Product recalled due to the presence of yellow oleander and its components in the product.
Helados Mexico Premium Ice Cream Minis Variety Pack 12 bars Strawberry, Coconut, Mango 1.5 FL OZ (44mL) Bards Net 18 FL OZ (528mL)
Tropicale Foods
Salmonella contamination
MK Cinnamon Powder, 45g, plastic bottle
Mak Trading Co.
Elevated levels of lead found in product
S.P Labs, Thyroid, USP, Rx only, For Manufacturing, Processing or Repackaging Use only, Specialty Process Labs, Phoenix, AZ, NDC #'s a) 81305-100-01, b)81305-100-02, c)81305-100-03
Specialty Process Labs
Failed Stability Specifications
Microbial contamination of a non-sterile product: potential Bacillus cereus contamination.
CGMP Deviations
S.P.Labs, Thyroid, Full Strength, Rx only, For Manufacturing, Processing or Repackaging Use Only, Specialty Process Labs, Phoenix, AZ 85034, NDC 81305-500-01.
Specialty Process Labs
Failed Stability Specifications
Failed Impurities/Degradation Specifications
Failed dissolution specifications: out-of-specification bempedoic acid dissolution at the 0-month timepoint.
Vancomycin Hydrochloride for Oral Solution, USP, 250 mg per 5 mL, packaged as (a) 80 mL bottle, NDC 69238-2261-3; (b) 150 mL bottle, NDC 69238-2261-7; (c)300 mL bottle, NDC 69238-2261-5; Rx only, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807
Amneal Pharmaceuticals of New York
Superpotent Drug: Due to overfilling of drug powder
Ingenia 1.5T S, Magnetic Resonance System.
Philips North America
Patient support table floor plate may be incorrectly installed.
Trilogy Evo Universal Ventilator, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients.
Philips Respironics
Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power.
Specific lots of Neria Soft Infusion Sets, which have been shipped into the US Market, have been shipped with the incorrect Instruction for Use (IFU) within the final pack. The IFU included is the IFU registered for the Rest of World (ROW) countries. The difference between the US IFU and the ROW IFU is the addition of an intended use section in the ROW IFU.
Achieva 1.5T, Magnetic Resonance System.
Philips North America
Patient support table floor plate may be incorrectly installed.
Intera 1.5T Omni/Stellar, Magnetic Resonance System.
Philips North America
Patient support table floor plate may be incorrectly installed.
Achieva 3.0T, Magnetic Resonance System.
Philips North America
Patient support table floor plate may be incorrectly installed.