HIGH
CPSC
Cranach Hardware Recalls Tip Restraint Kits for Tip-Over Hazard (2025)
Cranach Hardware
The recalled
nhtsa regulated Recalls
370 recalls tagged with “nhtsa regulated”.
HIGH
CPSC
Olympia Tools Recalls Pack-N-Stroll Premium Folding Utility Wagon for 2025 Entrapment and Falls Risk
Olympia Tools International
The utility
HIGH
Food & Beverages
HIGH
FDA FOOD
M.C.I. Foods Recalls 330 Cases of Cheese and Egg with Green Salsa Breakfast Burrito Over Listeria (H
Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria Monocytogenes
M.C.I. Foods
Cooked egg
Health & Personal Care
HIGH
Health & Personal Care
HIGH
FDA DEVICE
DERMASENSOR DermaSensor 10101 Diagnostic Device Recalled for 9 of 343 Units (2025)
Potential for device to not meet specifications resulting in incorrect results or delay of referral for patients.
DERMASENSOR
Potential for
Health & Personal Care
HIGH
FDA DRUG
Lannett NIACIN ER 1,000 mg Recall Affects 46,848 Bottles Nationwide (2025)
Lannett
Failed Dissolution
Health & Personal Care
HIGH
FDA DRUG
Major Pharmaceuticals Gabapentin 100 mg 10-Capsule Recall Nationwide 2025
Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity .
Gabapentin
Failed Impurities/Degradation
Health & Personal Care
HIGH
FDA DRUG
CA Botana Mineral Sunscreen Recall Covers 1,167 Tubes Over CGMP Deviations (2025)
MINERAL SUNSCREEN
CGMP Deviations
Health & Personal Care
HIGH
FDA DRUG
Elixir by Coco March Tinted Mineral Sunscreen SPF 50 Recalled for CGMP Deviations
SUNSCREEN
CGMP Deviations
Health & Personal Care
HIGH
FDA DRUG
STAQ Pharma Ketamine Hydrochloride Injection 50 mL Recall for Labeling Errors (2025)
Labeling: Incorrect or Missing Lot and/or Exp Date
STAQ Pharma
Labeling: Incorrect
Health & Personal Care
HIGH
FDA DRUG
Fasenra Benralizumab Injection Recall: 916 Pre-Filled Syringes Over Sterility Concern (2025)
Lack of Assurance of Sterility:
Fasenra
Lack of
Health & Personal Care
HIGH
FDA DRUG
Rising Pharma Carbidopa/Levodopa/Entacapone Tablets Recall 2,064 Bottles Nationwide (2025)
Rising Pharma Holdings
Product mix
Health & Personal Care
HIGH
FDA DRUG
Viona Pharmaceuticals Recalls 13,080 Tavaborole Topical Solution 5% Bottles (2025 Recall)
Zydus Lifesciences
Discoloration -
Vehicles & Parts
HIGH
NHTSA
VOLKSWAGEN ID. BUZZ 2025 Recall for Incorrect Instrument Panel Warning Light, 90A2
Volkswagen
An incorrectly
Health & Personal Care
HIGH
FDA DRUG
Camber Ketorolac Tromethamine Injection Recall 2025 for Glass Particulates
Presence of Particulate Matter: Particulate matter identified as glass
Ketorolac Tromethamine
Presence of
Health & Personal Care
HIGH
FDA DRUG
AFCO Hand Sanitizer 5515 Recalled for Methanol Risk Nationwide (2025)
cGMP deviations: The recall was initiated because required receipt testing of incoming alcohol components used to manufacture the listed hand sanitizers was not performed, so methanol risk could not be excluded.
AFCO
cGMP deviations:
Health & Personal Care
HIGH
FDA DRUG
Acella Doxycycline Hyclate 100 mg Recall 2025 for Dissolution Failure - 4,680 Bottles Nationwide
Failed dissolution specifications: Stability testing found that the lot did not meet dissolution specifications.
Doxycycline
Failed dissolution
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland 718096 Zenition 50 Interventional X-Ray System Recalled in 2025
Over time some systems may experience loss of imaging functionality and/or poor image quality due to potential corrosion of the Image Intensifier Television (IITV) control board.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Over time
Health & Personal Care
HIGH
FDA DRUG
Medline 222,800 Alcohol Prep Pads Recalled for Subpotent Drug (2025)
Medline Industries recalled 222,800 alcohol prep pads nationwide on Sept. 29, 2025 due to subpotent potency. The pads are 2-ply, 70% isopropyl alcohol. Stop using immediately and contact Medline or your healthcare provider for guidance.
Medline Industries
Subpotent Drug