living room Recalls

50 recalls tagged with “living room”.

Health & Personal Care
HIGH
FDA DEVICE

Philips CT Systems Brilliance 40/64 Channel and Ingenuity Flex Recalled for Couch Descent Risk (2025

Philips North America LLC is recalling 181 CT systems worldwide, including Brilliance CT 40 Channel 728235, Brilliance CT 64 Channel 728231, and Ingenuity Flex 728317. The patient support couch may descend to the lowermost position after a replacement. Hospitals and imaging centers should stop using the devices immediately and await recall instructions.

Philips
The patient
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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 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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Recalled Dearlomum retractable safety gate-black
HIGH
CPSC

Dearlomum Retractable Safety Gate Recall 2025 for Entrapment Hazard (SH20.006D)

Dearlomum retractable mesh safety gates sold on Amazon by Signbaby are recalled. The gates violate federal expansion gate standards because a child's torso can fit through the base opening, creating a risk of serious injury or death from entrapment. Stop using the recalled gates immediately and contact Signbaby for a full refund; disassemble, destroy the mesh, and email a photo to regcards.team@gm

Dearlomum
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal SA Recalls 1 Unit 40KW-FX.899 Mobile X-ray System Over Cleaning Hazard (2025)

Sedecal SA recalled 1 unit of the 40KW-FX.899 Mobile X-ray System distributed to CA, IL and NJ. The device is not water-resistant and must be cleaned strictly per the manual. Improper cleaning could cause adverse effects. Stop using the device and contact Sedecal SA or a healthcare provider for instructions.

Sedecal SA
Sedecal sent
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Food & Beverages
HIGH
FDA FOOD

PRIMO NO. 1 IN PRODUCE Recalled 89 Boxes of Sliced Cucumber for Salmonella Contamination (2025)

PRIMO NO. 1 IN PRODUCE recalled 89 boxes of sliced cucumber packaged in 2/10-lb boxes distributed to Virginia, New York, Pennsylvania and New Jersey after Salmonella contamination. The recall is active and classified as high risk. Consumers should not eat the product and should contact PRIMO NO. 1 IN PRODUCE for refund or replacement.

PRIMO NO. 1 IN PRODUCE
Product contaminated
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Tag Statistics

Total Recalls
50

Related Tags

fall hazardtip over riskstop use immediatelyreplacement availablereturn for refundfda regulatedcpsc regulatedinfant productadult productchemical hazardelectrical hazardkitchen