holiday product Recalls
154 recalls tagged with “holiday product”.
Instrumentation Laboratory GEM Premier 5000 GEM PAK Recall Affects 74 Units Worldwide
Teva Isotretinoin 40 mg Capsules Recalled for Superpotent and Subpotent Lots (D-0446-2026)
Teva Pharmaceuticals USA, Inc. recalls 8,376 isotretinoin 40 mg capsules distributed to FL, OH, PR and MS after FDA enforcement report flags superpotent and subpotent lots. Patients should stop use and contact their healthcare providers for guidance.
Olympus ShockPulse-SE Lithotripsy System Recall Expands to 55 Units in 5 Countries (2026)
GOLD STAR DISTRIBUTION Vaporizing Chest Rub Recall 2026 All Lots Nationwide
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Swan White Clear Alcohol Recall by Gold Star Distribution in 2026
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Gold Star Distribution Ice Gel 8oz 12-Count Recalled for CGMP Violations (2026)
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.

Primark Water Balloon Pumps Recall 5252801 Over Rupture Hazard (2025)
This recall involves Primark Water Balloon Pumps, which were sold in blue and pink. The pumps are shaped like a water bottle with a spray head. The product code 5252801 is printed on the price tag located on the back of the water balloon pump bottle.

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

Mallimoda Children's Pajama Sets Recalled Over Burn Hazard in 2025
Mallimoda recalled its children’s pajama sets sold on Amazon due to a burn hazard risk. The recall cites violations of mandatory sleepwear standards. Consumers should stop using the recalled sets and contact Mallimoda for a full refund.

Sanven Technology Recalls 3 Vevor Baby Swing Models for Suffocation Risk (2025)
GET TESTED INTERNATIONAL AB Heavy Metals Test Recall for 50 Units (2025)
Distribution without premarket approval/clearance.
GET TESTED INTERNATIONAL AB Kidney Test Recalled for 100 Units in 2025
Distribution without premarket approval/clearance.
GET TESTED INTERNATIONAL AB Blood Type Test Recalled for Lack of Premarket Approval (47 Units) 2025
Distribution without premarket approval/clearance.
Philips IntelliVue MX100 Patient Monitors Recalled for Alarm Failure (Z-0861-2026)
Potential issue where the IntelliVue monitors did not alarm.

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


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

DINBooonLUX 12-Inch Full-Size Mattress Recalled for Fire Hazard (2025)
DINBooonLUX recalled 12-Inch Full-Size Hybrid Mattresses sold on Amazon. The mattresses violate the mandatory flammability standard and pose a risk of serious injury or death in a fire. Stop using the mattress and contact DINBooonLUX for a full refund.
