holiday product Recalls

153 recalls tagged with “holiday product”.

Health & Personal Care
HIGH
FDA DEVICE

Instrumentation Laboratory Recalling 1,126 GEM PAK Cartridges for GEM Premier 5000 Over PCSND Errors

Instrumentation Laboratory issued a high-severity recall for 1,126 GEM PAK cartridges used with the GEM Premier 5000. The recall cites increased PCSND errors during warm-up that can cause consecutive GEM PAK ejections. The issue may delay patient results. Hospitals should halt use and follow manufacturer instructions immediately.

Instrumentation Laboratory
Confirmed customer
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Health & Personal Care
HIGH
FDA DEVICE

Olympus ShockPulse-SE Lithotripsy System Recall Expands to 55 Units in 5 Countries (2026)

Olympus Corp. of the Americas recalls 55 ShockPulse-SE Lithotripsy System units distributed internationally. Mis-wired component may create noise on the power supply and ultrasonic circuit. Hospitals and providers should stop using the device immediately and follow recall instructions. Notify Olympus or your healthcare provider for guidance.

Olympus
Mis-wired component-the
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Health & Personal Care
HIGH
FDA DRUG

GOLD STAR DISTRIBUTION Vaporizing Chest Rub Recall 2026 All Lots Nationwide

Gold Star Distribution is recalling all lots of its Vaporizing Chest Rub, 4 oz, 12-count, UPC 048155903319, distributed nationwide in the United States. The recall, number D-0283-2026, stems from CGMP deviations including insanitary conditions with rodent exposure/activity at the distribution center. Consumers and healthcare providers should stop using the product immediately and contact Gold Star

Gold Star Distribution
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

Gold Star Distribution Ice Gel 8oz 12-Count Recalled for CGMP Violations (2026)

Gold Star Distribution recalls 8oz Ice Gel 12-count sold nationwide after investigators found insanitary conditions at the distributor's facility. A CGMP deviation allowed rodent exposure at the distribution center. Consumers and healthcare providers should stop using this product immediately and await guidance from Gold Star Distribution.

Gold Star Distribution
CGMP Deviations:
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Food & Beverages
HIGH
FDA DRUG

Swan White Clear Alcohol Recall by Gold Star Distribution in 2026

Gold Star Distribution recalls Swan White Clear Alcohol, 50% ABV, 16 oz, 12 count, nationwide. FDA enforcement cites CGMP deviations and insanitary distribution-center conditions including rodent exposure. Stop using the product now and contact the distributor or a healthcare provider for guidance.

Swan
CGMP Deviations:
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Recalled Primark Water Balloon Pump (front)
MEDIUM
CPSC

Primark Water Balloon Pumps Recall 5252801 Over Rupture Hazard (2025)

Primark US recalls Primark Water Balloon Pumps due to rupture risk. The affected units were sold at Primark stores in the United States from March 2023 through July 2023 for about $6. Consumers should stop using the pumps immediately and return them to a Primark store for a full refund.

Primark
The water
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Recalled Ojaswi 12-Drawer Dressers in gray (front)
HIGH
CPSC

Ebern Designs Ojaswi 12-Drawer Dressers Recalled for Tip-Over Risk (2025)

Wayfair sold the Ebern Designs Ojaswi 12-Drawer Dressers from January 2025 through October 2025 for about $75. The recall covers models HD011BL-SL and HD011WH-SL. The dressers measure 39 inches by 43 inches by 12 inches and weigh about 31.7 pounds. They can tip over if not anchored to a wall, posing a risk of serious injury or death to children. Consumers should stop using the recalled dressers if

Ebern Designs
The recalled
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Recalled Vevor Baby Swing in White/Gray with White Base and Mosquito Net, Model Number BB501
HIGH
CPSC

Sanven Technology Recalls 3 Vevor Baby Swing Models for Suffocation Risk (2025)

Sanven Technology recalls 3 Vevor Baby Swing models on 2025-11-06 for a suffocation risk linked to an incline greater than 10 degrees. The swings carry the VEVOR trademark and are labeled as Multi-Function Electric Swing with model numbers BB501K, BB702A, and BB005. Consumers should stop using the swings immediately and contact Sanven Technology for a full refund.

Sanven Technology
The swings
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Health & Personal Care
HIGH
FDA DEVICE

GET TESTED INTERNATIONAL AB Heavy Metals Test Recall for 50 Units (2025)

GET TESTED INTERNATIONAL AB recalled 50 units of Heavy Metals Test distributed nationwide in the United States. The device was distributed without premarket FDA approval or clearance. Stop using the device immediately and contact GET TESTED INTERNATIONAL AB for instructions.

GET TESTED INTERNATIONAL AB
Distribution without
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Health & Personal Care
HIGH
FDA DEVICE

GET TESTED INTERNATIONAL AB Kidney Test Recalled for 100 Units in 2025

GET TESTED INTERNATIONAL AB recalled 100 Kidney Test devices sold nationwide in the United States. The recall cites distribution without premarket approval or clearance. Healthcare providers and patients should stop using the device immediately and follow manufacturer instructions.

GET TESTED INTERNATIONAL AB
Distribution without
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Health & Personal Care
HIGH
FDA DEVICE

GET TESTED INTERNATIONAL AB Blood Type Test Recalled for Lack of Premarket Approval (47 Units) 2025

GET TESTED INTERNATIONAL AB recalled 47 Blood Type Test units distributed nationwide in the United States after discovering the device was distributed without FDA premarket approval or clearance. The hazard is distribution without FDA premarket approval or clearance. Patients and healthcare providers should stop using the device immediately and contact GET TESTED INTERNATIONAL AB for instructions.

GET TESTED INTERNATIONAL AB
Distribution without
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Health & Personal Care
HIGH
FDA DEVICE

Philips IntelliVue MX100 Patient Monitors Recalled for Alarm Failure (Z-0861-2026)

Philips North America recalled 1,913,441 IntelliVue MX100 patient monitors due to potential alarm failure. The recall is active as of December 2025. The manufacturer warns patients and healthcare providers to stop using affected devices and follow recall instructions. Contact Philips North America LLC for guidance.

Philips North America
Potential issue
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Recalled Polaris Model Year 2025 Ranger XP 1000 NorthStar
HIGH
CPSC

Polaris Recalls 2025-2026 Ranger XP 1000 NorthStar UTVs for Fire Hazard

Polaris Industries recalled certain VINs of 2025-2026 Ranger XP 1000 NorthStar and Ranger Crew XP 1000 NorthStar UTVs sold through Polaris dealers nationwide for between $28,000 and $38,000. An improperly routed alternator cable can contact the negative battery post, creating an electrical short and a fire risk. Owners should immediately stop using the recalled vehicles and contact Polaris for a免费

Polaris Industries
An improperly
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Recalled Halloween-themed Skeleton Wax Candle
HIGH
CPSC

Kroger Recalls Halloween Skeleton Wax Candles for Fire Hazard (2025)

The Kroger Co. recalls Halloween-themed Skeleton Wax Candles sold at Kroger stores due to a fire hazard. The candle contains flammable ornaments that create a burn risk. Consumers should stop using the candle immediately and return it to any Kroger store for a full refund.

Kroger
The candle
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Recalled Grundens Youth Zenith 282 Jacket (navy)
HIGH
CPSC

Grundens Recalls Youth Clipper 282 and Zenith 282 Jackets Over Drawstrings Strangulation Hazard (202

Grundens has issued an active recall for the Youth Clipper 282 Jacket and the Youth Zenith 282 Jacket in youth sizes 8 through 12. The jackets have hood drawstrings that can catch on objects, creating a risk of strangulation. Consumers should stop using the jackets immediately and contact Grundens for a full refund or a 20% store credit after removing the drawstrings.

Grundens
A drawstring
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical IV Administration Sets Recalled for Backflow Risk and Occlusion (2025)

B Braun Medical Inc. recalls 111,312 IV Administration Sets worldwide, including US and international markets, due to backflow risk and occlusion. The recall affects catalog numbers 490193 and 490326, used with Infusomat Space, Outlook, and Vista Basic pumps. Stop using immediately and follow recall instructions for refunds or replacements.

B Braun Medical
Potential for
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Tag Statistics

Total Recalls
153

Related Tags

electrical hazardchemical hazardsuffocation riskinfant producttoddler productadult productelderly productpet relatedcpsc regulatedfda regulatednhtsa regulatedimmediate action
    holiday product Recalls | RecallRadar