CRITICAL
bathroom Recalls
119 recalls tagged with “bathroom”.
Health & Personal Care
HIGH
FDA DRUG
CA Botana Sunscreen Flawless Skin Fluid Tint SPF 50 Recall 2025
CA Botana International recalls Sunscreen Flawless Skin Fluid Tint SPF 50 after CGMP deviations. The recall covers 1,401 tubes distributed to California, Colorado, Florida, Puerto Rico and Washington. Stop using the product and contact CA Botana for guidance.
CA Botana International
CGMP Deviations
Food & Beverages
HIGH
FDA FOOD
Aldi Happy Farms Italian Style Shredded Cheese Recall 2025 — 1,900 Cases Over Metal Fragments
Great Lakes Cheese Co. Inc. recalls 1,900 cases of Happy Farms by Aldi Italian Style shredded cheese. The recall covers 12 oz bags distributed across 30 states and Puerto Rico. The hazard is potential metal fragments from supplier raw material.
Happy Farms
Potential metal
Health & Personal Care
HIGH
FDA DRUG
Church & Dwight Zicam Elderberry Medicated Fruit Drops Recalled for Label Mix-Up (21,912 Bottles, 0
Labeling: Label Mix-up: The product in the bottle contains elderberry and the label failed to indicate the inclusion of elderberry as an ingredient.
Zicam
Labeling: Label
Health & Personal Care
HIGH
FDA DRUG
Acuity Specialty Products Hand Sanitizer Recalled for Methanol Risk Due to Unperformed Component-LOT
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.
Acuity Specialty Products
cGMP deviations:
Health & Personal Care
HIGH
FDA DRUG
Ascend Laboratories Recalls Atorvastatin Calcium 80 mg Tablets (90-Count & 500-Count) for Failed Dil
Ascend Laboratories
Failed Dissolution
Health & Personal Care
HIGH
FDA DEVICE
B Braun Medical SESK Pain Management Tray Recall Affects 2,450 Units Nationwide (2025)
Potential for the lid of the catheter connector to be in the incorrect position.
B Braun Medical
Potential for
Health & Personal Care
HIGH
FDA DRUG
Glenmark Azelaic Acid Gel Recall Affects 13,824 Tubes Sold Nationwide in 2025
CGMP Deviations: Market complaints received for gritty texture (grainy)
Glenmark Pharmaceuticals
CGMP Deviations:
Health & Personal Care
HIGH
FDA DRUG
Private Label Skin Care Micronized Benzoyl Peroxide Gel Recall Expands for Benzene Contamination
Chemical Contamination: This recall has been initiated due to elevated levels of benzene that was discovered during post consume awareness with benzoyl peroxide products.
Private Label Skin Care
Chemical Contamination:
Health & Personal Care
HIGH
FDA DRUG
Torrey Pines Benzaderm BPO Cleanser 10% Recall Over Benzene Contamination, 2025
Torrey Pines Dermatology & Laser Center's Benzaderm BPO Cleanser recall remains active. The FDA-listed recall covers benzoyl peroxide cleanser lot numbers 58170A and 58172A with expiration 09/2025. Consumers should stop use and contact the recall coordinator.
Private Label Skin Care
Chemical Contamination:
Health & Personal Care
HIGH
FDA DEVICE
Olympus BF-PE2 Bronchoscope Recall Expands with 4,289 Units Aboard Outside US
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
Olympus Corporation of the Americas
Additional IFU
Health & Personal Care
HIGH
FDA DEVICE
GE Medical Systems AW Server 2.0, AW Server 3.0, 3.1, 3.2 Recalled For Security Breach Risk (2025)
Firm has identified a security vulnerability in AW Server products. If exploited, a malicious actor could compromise the confidentiality, integrity, and availability of patient data.
GE Medical Systems
Firm has
Food & Beverages
HIGH
FDA FOOD
Pacific Coast Producers Fruit Cocktail Recalled for Lead Contamination in 15 oz Cans (609 cases)
Potential contamination with heavy metal (Lead).
Pacific Coast Producers
Potential contamination
Health & Personal Care
HIGH
FDA DRUG
Zydus Chlorpromazine Hydrochloride 200 mg Recall Expands Nationwide Over CGMP Deviations
CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit
Chlorpromazine Hydrochloride
CGMP Deviations:
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD10 Recalled for BIOS Battery Startup Failure (2,317 Units Worldwide, 2025)
Philips Medical Systems Nederland
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Inpeco FlexLab X System Potassium Test System Recalled for Unvalidated Hemolysis, Icterus, Lipemia H
Inpeco S.A.
The FlexLab
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland Blames BIOS Battery Design Flaw in Allura Centron 722400 Recall (Z
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The BIOS
Health & Personal Care
HIGH
FDA DRUG
Major Pharmaceuticals Sulfamethoxazole and Trimethoprim 800 mg/160 mg 100-Tablets Recall 2025
Presence of a Foreign Substance: A specific lot of auxiliary polyester coil, used in product packaging by manufacturer (Amneal Pharmaceuticals LLC) was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Sulfamethoxazole and Trimethoprim
Presence of
Health & Personal Care
HIGH
FDA DEVICE
ImaCor ClariTEE Miniaturized TEE Probe CLT-010 Recalled Over Reversed Articulation Risk (2025)
Production assembly error resulting in the potential for reversed articulation, where moving the lever forward caused the probe tip to anteflex rather than retroflex, and vice versa.
ImaCor
Production assembly
Health & Personal Care
HIGH
FDA DEVICE
Northeast Scientific Recalled 561 Units of NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy C
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
Northeast Scientific
Potential for