bathroom Recalls

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

Yeeluzan Pool Drain Covers Recalled for Entrapment Risk in 2-Pack (2026)

Yeeluzan recalled two-pack pool drain covers sold on Amazon. The covers measure 8.7 inches in diameter and weigh 1.7 pounds. They are white ABS plastic and packaged as two-packs. Pool owners should stop using these recalled covers and request a full refund.

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

Sunnyyes LED Mini Lights Recalled for Battery Ingestion Risk, Despite Reese’s Law Violations

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

Lanreotide Injection recall: Cipla USA lanreotide acetate pre-filled syringes recalled for sterility

Lack of Assurance of Sterility: Due to an FDA observation at the contract manufacturing site for deficiencies in their visual inspection procedure.

Fresenius Kabi 5% Dextrose Injection Recall for Sterility Concerns (2026) Affecting US Nationwide, R

Lack of Assurance of Sterility

Fresenius Kabi 0.9% Sodium Chloride Injection Recalled for Lack of Sterility Assurance (2026)

Lack of Assurance of Sterility

Fresenius Kabi 5% Dextrose Injection Recalled for Lack of Sterility Assurance (2026)

Lack of Assurance of Sterility

Cook Medical Spectrum Central Venous Tray Recalled Over Expired Shelf-Life Labels (2026)

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

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

Product labeling includes a fetal indication for use that is not cleared under its 510(k).

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

Lack of Assurance of Sterility

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

Lack of Assurance of Sterility

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

Lack of Assurance of Sterility

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

Lack of Assurance of Sterility

Olympus SOLTIVE Pro Laser System Recall 2026 — 32 Units Worldwide

Medline NAMIC Angiographic Rotating Adaptor Syringes Recalled in Class I Action for 79,843 Units

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

Medline NAMIC Angiographic Rotating Adaptor Syringes Recalled in 2,980 Kits Worldwide

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

Surreal Brands Recalls Tubby Tots Bath Foam Sets Over Impact Hazard

Surreal Brands recalled Tubby Tots Fizzy Flask Bath Magic bath foam sets on February 26, 2026. Moisture can cause pressure to build up, posing an impact hazard. Consumers should stop using these products immediately and seek a refund.

Mentor Texas CPX 4 US Breast Tissue Expanders Recall 2026

Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.