MEDIUM
CPSC
DT Swiss Recalls Carbon Wheels Over Crash Hazard Affecting 2740000 ID Codes and Higher (2025)
DT Swiss
A defect
bathroom Recalls
119 recalls tagged with “bathroom”.
Health & Personal Care
HIGH
FDA DRUG
Ascend Laboratories Recalls ARIPIPRAZOLE 10 mg Tablets Over Superpotent Drug Risks (2025)
ARIPIPRAZOLE
Superpotent drug
Health & Personal Care
HIGH
FDA DRUG
Granules Pharmaceuticals Recalls 3,384 Bottles of Dextroamphetamine ER Capsules for Impurity Issues
Granules Pharmaceuticals
Failed Impurities/Degradation
Health & Personal Care
HIGH
FDA DEVICE
Siemens Biograph mMR PET-MRI Recall 2025 for Ice Blockage Risk in Venting System (23 Units)
Siemens
There is
Health & Personal Care
HIGH
FDA DEVICE
Siemens MAGNETOM Skyra MRI System Recall Covers 182 Units Over Ice Blockage Risk
Siemens Medical Solutions USA
There is
Health & Personal Care
HIGH
FDA DEVICE
Siemens MAGNETOM Lumina MRI System Recall Covers 71 Units Worldwide for Ice Blockage Risk
Siemens Medical Solutions USA recalled 71 MAGNETOM Lumina MRI systems worldwide, including US and 50+ countries, due to ice blockage in the magnet venting system that could cause a helium leak during a quench.
Siemens Medical Solutions USA
There is
Health & Personal Care
HIGH
FDA DRUG
Unichem Pharmaceuticals USA Cyclobenzaprine Recall for Label Mix-Up Affects 230 Bottles (2025)
Labeling: Label Mix Up; Bottles of Meloxicam USP, 7.5mg, 90-count tablets (yellow in color), were labeled as Cyclobenzaprine Hydrochloride Tablets USP, 10 mg 90-count tablets (blue in color).
CYCLOBENZAPRINE HYDROCHLORIDE
Labeling: Label
Health & Personal Care
HIGH
FDA DRUG
TopCare Health 70% Isopropyl Alcohol Recall Expands to 60 Bottles Nationwide (2025)
Cross Contamination with Other Products.
TopCare Health
Cross Contamination
Health & Personal Care
HIGH
FDA DEVICE
Frontier Devices Recalls 160 301.912S2 12 mm Distraction Pin Over Unvalidated Shelf-Life Labeling (Z
Labeling includes shelf life that has not been validated.
Frontier Devices
Labeling includes
HIGH
Health & Personal Care
HIGH
FDA DEVICE
Frontier Devices 301.912S1 12 mm Distraction Pin Recall Expanded to 3,790 Units (Rx Only)
Labeling includes shelf life that has not been validated.
Frontier Devices
Labeling includes
Health & Personal Care
HIGH
FDA DEVICE
Frontier Devices Recalls 2,700 REF 301.914S1 14 mm Distraction Pins (2025)
Labeling includes shelf life that has not been validated.
Frontier Devices
Labeling includes
Health & Personal Care
HIGH
FDA DRUG
READYPREP PVP Iodine 10% Topical Antiseptic Recalled for Subpotent Drug (Medline)
FDA recalls READYPREP PVP, povodone-iodine 10% topical antiseptic. Medline Industries issued the nationwide recall. Subpotent drug is the reason. Consumers should stop using the product immediately.
POVIDONE-IODINE
Subpotent drug
Health & Personal Care
HIGH
FDA DRUG
B. Braun Sodium Chloride Injection 1000 mL Recalled nationwide for particulates (Class I)
B. Braun Medical Inc. recalls 47,148 containers of 0.9% Sodium Chloride Injection USP nationwide after detecting particulate matter. The Class I recall affects bottles with NDC 0264-7800-09. Stop using and contact providers for guidance.
B. Braun Medical Inc.
Presence of
Health & Personal Care
HIGH
FDA DRUG
B. Braun Lactated Ringers Injection 46,032 Containers Recalled Over Particulate Matter
B Braun Medical
Presence of
Health & Personal Care
HIGH
FDA DRUG
Novartis/Sandoz Otic Suspension Recalled for Temperature Abuse (D-0626-2025)
CIPROFLOXACIN AND DEXAMETHASONE
Temperature Abuse
Health & Personal Care
HIGH
FDA DEVICE
Philips Ingenuity CT Brazil 728325 CT System Recalled for 3 Units in 2025
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
Philips
The patient
Health & Personal Care
HIGH
FDA DEVICE
Beckman Coulter UniCel DxH 800 Hematology Analyzers Recalled for High Hemoglobin Readings in High-WB
Hematology analyzers configured with HGB photometers may result in erroneously high hemoglobin (HGB) results on samples with elevated white blood cell (WBC) counts.
Beckman Coulter
Hematology analyzers
Health & Personal Care
HIGH
FDA DEVICE
Penner Patient Care Penner Pacific Bathing Spa Recalled for Missing UDI (25 Units, 2025)
The device does not bear a unique device identifier.
Penner Patient Care
The device
Health & Personal Care
HIGH
FDA DEVICE
Penner Pacific Bathing Spa Recalled for Missing Unique Device Identifier (UDI) in 206 Units
The device does not bear a unique device identifier.
Penner Patient Care
The device
Tag Statistics
Total Recalls
119