bathroom Recalls

29 recalls tagged with “bathroom”.

Recalled Arey, Not Today, Grey (180ct) - front
HIGH
CPSC

Vitaquest International Recalls Multiple Iron Supplements for Child-Resistant Packaging Violations (

Vitaquest International recalled Arey Not Today iron supplements sold at retailers nationwide after determining the products do not meet the Poison Prevention Packaging Act's child-resistant packaging requirement. The noncompliant packaging creates a poisoning risk to young children if ingested. Consumers should stop using the products immediately and contact Vitaquest for a free child-resistant替换

Vitaquest International LLC of West Caldwell, New Jersey
The dietary
Read more
Recalled TecFlox Topical Solution - hair and beard growth serum bottle
HIGH
CPSC

TecFlox Minoxidil Topical Solution Hair Serum Recalled for Child Poisoning Risk (2026)

TecFlox recalled its Minoxidil Topical Solution hair growth serum bottles on April 2, 2026. The packaging is not child-resistant, violating the Poison Prevention Packaging Act. Consumers should stop using the product immediately, store it out of reach of children, and email TecFloxrecall@outlook.com to receive free replacement bottles. Only bottles with serum remaining will be replaced; dispose of

TecFlox Hair and Beard Growth Serum Bottles
The hair
Read more
Recalled Wagner Model 905e Auto Steamer, pictured with included accessories
HIGH
CPSC

Wagner Spray Tech Recalls 900-Series Power Steamers Over Burn Hazard (2026)

Wagner Spray Tech recalls 900 Series power steamers, including the 905e Auto Steamer, 915e On-Demand Power Steamer, and 925e Steam Machine Elite Steamer. The recall cites a burn hazard from an overheating hose and hot-water expulsion from the nozzle. Consumers should stop using the recalled steamers immediately and contact Wagner for a free repair kit.

Wagner Spray Tech
The attached
Read more
Health & Personal Care
HIGH
FDA DEVICE

Koven Technology BiDop 3 Pocket Doppler ES-100V3 Recalled for Fetal Labeling Issue (2026)

Koven Technology recalled 34 BiDop 3 Pocket Dopplers with BT2M20S8C fetal probes nationwide after regulators found the fetal indication on the labeling was not cleared under 510(k). The defect is labeling that misrepresents fetal use. Healthcare providers and patients should stop using the devices and follow recall instructions from the manufacturer.

Koven Technology
Product labeling
Read more
Health & Personal Care
HIGH
FDA DRUG

Goodsense Eye Drops Original Formula Recall 378,144 Bottles Nationwide 2026

Goodsense Eye Drops Original Formula, distributed nationwide, has recalled 378,144 sterile bottles in 2026 due to lack of assurance of sterility. The sterile ophthalmic solution may be contaminated. Consumers and healthcare providers should stop using immediately and contact K.C. Pharmaceuticals for refunds or replacements.

Goodsense Eye Drops Original Formula
Lack of
Read more
Health & Personal Care
HIGH
FDA DRUG

KC Pharmaceuticals Recalled Sterile Eye Drops AC 182,424 Bottles Nationwide (2026)

KC Pharmaceuticals recalled 182,424 Sterile Eye Drops AC bottles sold nationwide under multiple brands including Quality Choice Eye Drops Irritation Relief and Goodsense Ultra Lubricant Eye Drops. The recall cites a lack of assurance of sterility. Consumers should stop using the product immediately and contact KC Pharmaceuticals for guidance.

Quality Choice Eye Drops Irritation Relief
Lack of
Read more
Health & Personal Care
HIGH
FDA DRUG

Quality Choice Eye Drops and Foster & Thrive Eye Drops Recalled for Sterility in 303,216 Bottles (24

Quality Choice Moisturizing Relief Eye Drops and Foster & Thrive Advanced Relief Eye Drops are recalled after 303,216 bottles distributed nationwide through Walgreens, CVS and other retailers lack sterility. The defect is lack of assurance of sterility. Consumers should stop using the products immediately and contact KC Pharmaceuticals for guidance.

Quality Choice
Lack of
Read more
Health & Personal Care
HIGH
FDA DRUG

ARTIFICIAL TEARS Dry Eye Relief Eye Drops Recalled in 2026 Over Sterility Concerns

More than 1.02 million bottles of Dry Eye Relief Eye Drops across multiple brands were recalled nationwide on March 3, 2026. The products were distributed by KC Pharmaceuticals and sold at retailers including Rite Aid, Meijer and H-E-B. The FDA notice cites a lack of assurance of sterility as the reason for the recall. Stop using these products immediately and contact KC Pharmaceuticals for next‑s

ARTIFICIAL TEARS
Lack of
Read more
Health & Personal Care
HIGH
FDA DEVICE

Olympus SOLTIVE Pro Laser System Recall 2026 — 32 Units Worldwide

Olympus recalled 32 SOLTIVE Pro SuperPulsed Laser System units distributed worldwide after a defect in the 24V power supply may render the device inoperable. The defect can cause smoke or a burning smell, but the issue is contained within the laser console enclosure and self-extinguishing. Stop using the device and follow the manufacturer’s recall instructions.

Olympus
Following a
Read more
Health & Personal Care
HIGH
FDA DEVICE

Mentor Texas CPX 4 US Breast Tissue Expanders Recall 2026

Mentor Texas, LP recalled CPX 4 US Breast Tissue Expanders with Suture Tabs worldwide on February 18, 2026. The recall covers models SCPX-107MH, SCPX-117MH, SCPX-127MH, SCPX-135MH, SCPX-146MH and SCPX-156MH. Infusion sets may include a dull needle tip that is difficult to advance and may break. Stop using the device and follow recall instructions from the manufacturer, with recall notification by-

Mentor Texas
Infusion sets
Read more
Recalled PurSteam Elite Travel Steamer – Model PS-510
HIGH
CPSC

Aterian Recalls PurSteam Elite Travel Steamers and Mighty Lil Steamers for Burn Hazard (2026)

Aterian recalls PurSteam Elite Travel Steamers and PurSteam Mighty Lil Steamers sold after December 2020 due to a burn risk. The steamers can expel hot water from the steam nozzle during use. Affected consumers should stop using the recalled steamers and submit a recall request at recall.pursteam.com for a full refund, which requires cutting the cord and uploading a photo of the steamer with its C

Aterian
The steamers
Read more
Health & Personal Care
HIGH
FDA DRUG

Medi-First Antiseptic Wipes Recalled for CGMP Deviations in 2026, 100 Wipes per Box

ACME United Corporation recalled Medi-First Antiseptic Wipes sold nationwide in the United States. The recall cites CGMP deviations that could affect product quality. Consumers and healthcare providers should stop using the wipes immediately and contact ACME United Corporation or a healthcare provider for guidance.

Medi-First Antiseptic Wipes
CGMP Deviations
Read more
Health & Personal Care
HIGH
FDA DRUG

ACME UNITED Recalls Max Packaging Antibacterial Towelette for CGMP Deviations (2026)

ACME UNITED recalled Max Packaging Antibacterial Towelette nationwide in the United States after CGMP deviations were identified. Manufacturing quality deviations prompted the recall, classified as Class II and labeled as high hazard. Stop using the product immediately and contact ACME UNITED CORPORATION or your healthcare provider for guidance.

ACME UNITED
CGMP Deviations
Read more
Health & Personal Care
HIGH
FDA DRUG

Med-Nap Cleansing Towelettes Recall 2026 for CGMP Deviations

Med-Nap Cleansing Towelettes, manufactured by Acme United Corporation, were recalled nationwide on January 20, 2026. The recall cites CGMP deviations in manufacturing for benzalkonium chloride 0.13% towelettes. Consumers and healthcare providers should stop using the product immediately and contact Acme United for guidance.

Med-Nap Cleansing Towelettes
CGMP Deviations
Read more
Health & Personal Care
HIGH
FDA DRUG

ACME United BZK Antiseptic Towelettes Recall for CGMP Deviations (2026)

ACME United Corporation recalled BZK Antiseptic Towelettes sold for Food Service Resources nationwide after CGMP deviations were found. The recall is Class II and high risk. Consumers and healthcare providers should stop using this product immediately and follow recall guidance.

ACME United
CGMP Deviations
Read more
Health & Personal Care
HIGH
FDA DRUG

Dukal BZK Antiseptic Towelettes Recalled for CGMP Deviations (2026)

Nationwide recall of Dukal BZK Antiseptic Towelettes due to CGMP deviations. The products are manufactured for Dukal, LLC in Ronkonkoma, NY and distributed across the United States. Stop using immediately and contact ACME United Corporation for guidance.

Dukal
CGMP Deviations
Read more
Health & Personal Care
MEDIUM
FDA DRUG

Green Guard Antiseptic Wipes Recall 2026 Over CGMP Deviations

Green Guard Antiseptic Wipes, distributed nationwide by ACME United Corporation, are being recalled as of January 20, 2026. FDA enforcement cites CGMP deviations in manufacturing for the benzalkonium chloride wipes, NDC 47682-056-73. Consumers and healthcare providers should stop using the product immediately and contact ACME United for guidance on refunds or replacements.

Green Guard Antiseptic Wipes
CGMP Deviations
Read more
12
Next

Tag Statistics

Total Recalls
29

Related Tags

poisoning riskimmediate actionstop use immediatelyfederal law violationcpsc regulatedadult productinfant productkitchenchemical hazardreplacement availablereturn for refundsuffocation risk