bathroom Recalls

119 recalls tagged with “bathroom”.

Health & Personal Care
HIGH
FDA DEVICE

Penner Patient Care's Penner Pacific Bathing Spa Recalled for Missing UDI in 21 Units (2025)

Penner Patient Care, Inc. recalled 21 Penner Pacific Bathing Spa units distributed nationwide in the United States after discovering the devices do not bear a unique device identifier. The missing UDI hinders traceability for adverse events and recalls. Consumers should stop using the devices and contact Penner Patient Care for instructions.

Penner Patient Care
The device
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Health & Personal Care
HIGH
FDA DEVICE

Penner Pacific Bathing Spa Recall: 10 Units Missing UDI (2025)

Penner Patient Care recalled 10 Penner Pacific Bathing Spa units nationwide on 2025-08-13 after regulators flagged the device lacks a unique device identifier. The device does not bear a unique device identifier. Patients and healthcare providers should stop using the device immediately and follow the manufacturer’s recall instructions.

Penner Patient Care
The device
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Health & Personal Care
HIGH
FDA FOOD

Hi-Tech Pharmaceuticals L-Glutamine Ultra Pure Powder Recall: 85,950 Units (2025)

Hi-Tech Pharmaceuticals recalled 85,950 units of L-Glutamine Ultra Pure Powder distributed to multiple retailers after FDA enforcement over unapproved drug claims. The product’s labeling asserts drug-like benefits without FDA approval. Consumers should not consume the product and should contact Hi-Tech Pharmaceuticals for refund or replacement by mail to 6015-B Unity Drive, Norcross, GA 30071.

Hi-Tech Pharmaceuticals
Unapproved Drug
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Health & Personal Care
HIGH
FDA FOOD

Hi-Tech Pharmaceuticals Formutech Nutrition Joint Formula Recalled for Unapproved Drug Claims (2025)

Hi-Tech Pharmaceuticals recalled 85,950 units of Formutech Nutrition Flexible Joint Formula with Cissus Quadrangularis sold nationwide after regulators flagged unapproved drug claims. The product claims to support tendons and muscles and promote healthy cartilage, which regulators say is not approved. Consumers who purchased the supplement should not use it and should await refund or replacement,'

Hi-Tech Pharmaceuticals
Unapproved Drug
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Food & Beverages
HIGH
FDA FOOD

M.O.M Enterprises Recalls 85,248 Organic BABY Bedtime Drops Over Spoilage Risk (2025)

M.O.M Enterprises recalled 85,248 units of Organic BABY bedtime drops sold through Multiple Retailers in 31 states. The product is a liquid dietary supplement for infants aged 4 months and older and may spoil due to yeast contamination. Consumers should not consume the product and should seek a refund or replacement from M.O.M Enterprises, LLC.

M.O.M Enterprises
Potential for
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Recalled Cosco 2-Step Kitchen Stepper model 11349WHG1E
MEDIUM
CPSC

Cosco 2-Step Kitchen Stepper Recall 2025 — 10 Models Affected

Dorel Home Furnishings recalls Cosco 2-Step Kitchen Steppers sold at multiple retailers after reports that the safety bar can detach or break during use. The recall covers 10 model numbers. Consumers should stop using the safety bar immediately and contact Dorel for a free repair kit.

Dorel Home Furnishings
The safety
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Health & Personal Care
HIGH
FDA DRUG

Sucralfate Tablets Recall Expanded After CGMP Deviations; 26,992 Blister Packs Affected

A recall is active for Sucralfate Tablets, USP 1 gram distributed by American Health Packaging. The firm filed for Chapter 11 in September 2024, triggering CGMP deviations and questions about product identity, strength, quality and purity. The recall affects 26,992 blister packs distributed nationwide. Stop using the product and contact Amerisource Health Services or your clinician for guidance.

SUCRALFATE
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DEVICE

Ortho-Clinical Diagnostics LAC Slides Recalled Over Calibration Failures on VITROS Systems

VITROS Chemistry Products LAC Slides recalled after calibration failures on VITROS XT 3400 and VITROS XT 7600 systems. The recall covers catalog 8433880 with 2,908 units distributed nationwide in the US. Manufacturers warn that coating 0130 and above with Condition Code TH4-63J elevates calibration failures, delaying lac test results and potentially impacting patient management. Health providers,病

Ortho-Clinical Diagnostics
VITROS Chemistry
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Health & Personal Care
HIGH
FDA DEVICE

Quidel Dipstick Strep A Tests Recalled for Potential False Positives (Z-2545-2025)

Quidel recalls 22,470 Rapid Strep A Dipstick tests sold worldwide, including multiple U.S. states. The dipstick test may yield false positive results. Health providers and patients should stop using the device immediately and follow recall instructions. Check with Quidel for refund or replacement options.

Quidel
Dipstick strep
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal MobileDiagnost wDR 2.2 Recall for 1,198 Units in 2025

Sedecal recalled 1,198 MobileDiagnost wDR 2.2 mobile X-ray systems distributed in California, Illinois and New Jersey. The company reminded users the equipment is not water-resistant and must be cleaned strictly according to the manual. Improper cleaning could have consequences outlined by Sedecal. Health care providers should stop using the device immediately and follow recall instructions.

Sedecal
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal SA Recalls Shimadzu RF.004 Mobile X-ray System in 2025

Sedecal SA is recalling the Shimadzu RF.004 Mobile X-ray System after warnings that the device is not water-resistant and must be cleaned strictly according to the manual. Hospitals in California, Illinois, and New Jersey are affected. Stop using the device and follow recall instructions.

Sedecal SA
Sedecal sent
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Tag Statistics

Total Recalls
119

Related Tags

fda regulatedmandatory standard violationimmediate actionstop use immediatelyreturn for refundreplacement availableadult productelectronicbattery poweredlithium batterycpsc regulatedholiday product