holiday product Recalls

37 recalls tagged with “holiday product”.

Health & Personal Care
HIGH
FDA DEVICE

Olympus OER-Pro Endoscope Reprocessor Recall for 3,354 Units Over MAJ-1443/1444 Compatibility (2026)

Olympus Corporation of the Americas recalled 3,354 units of the OER-Pro endoscope reprocessor on February 12, 2026. MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. Hospitals and clinics should stop using the device immediately and follow the manufacturer’s recall instructions.

Olympus Corporation of the Americas
The MAJ-1443
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Health & Personal Care
HIGH
FDA DEVICE

Burlington Medical Blockers Recalled for Attenuation Degradation in 51 Units Worldwide (2026)

Burlington Medical recalled 51 Blocker devices sold worldwide after a recall notice. The devices may degrade attenuation over time, shortening their lifespan. Stop using the devices immediately and follow the manufacturer’s recall instructions. Contact Burlington Medical, LLC or your healthcare provider for guidance. Distribution is worldwide.

Burlington Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Burlington Medical Leg Wraps Recall: 103 Units Worldwide in 2026

Burlington Medical, LLC recalled 103 leg wrap devices distributed worldwide through multiple retailers. The recall cites attenuation degradation over time that could shorten the devices' lifespan. Healthcare providers and patients should stop using them immediately and follow the manufacturer's recall instructions.

Burlington Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Abiomed Impella RP Recall 179 Units for Sensor Drift Risk (2026)

Abiomed recalled 179 Impella RP devices worldwide after a differential pressure sensor may drift. The fault can cause sensor values to drift, potentially affecting patient care. Stop using the device immediately and follow the recall instructions, including contacting Abiomed or your healthcare provider.

Abiomed
Differential pressure
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Food & Beverages
LOW
FDA FOOD

Mangalm Tops GOLD Stuffed Red Chilli Pickle Recall for Possible Erucic Acid Adulteration (2026)

Mangalm LLC recalled 40 cases of Tops GOLD Stuffed Red Chilli Pickle, 31.74 oz cans, distributed in California, Nevada, Oregon, Utah and Washington. The recall is due to potential adulteration with erucic acid from mustard oil. Consumers should not consume this product and should contact Mangalm LLC by email for a refund or replacement.

Mangalm
Potential adulteration
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Health & Personal Care
MEDIUM
FDA DRUG

Green Guard Antiseptic Wipes Recall 2026 Over CGMP Deviations

Green Guard Antiseptic Wipes, distributed nationwide by ACME United Corporation, are being recalled as of January 20, 2026. FDA enforcement cites CGMP deviations in manufacturing for the benzalkonium chloride wipes, NDC 47682-056-73. Consumers and healthcare providers should stop using the product immediately and contact ACME United for guidance on refunds or replacements.

Green Guard Antiseptic Wipes
CGMP Deviations
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Health & Personal Care
HIGH
FDA DRUG

Dynarex Obstetrical Towelettes Cleanser Recall 2026 for CGMP Deviations

Dynarex Obstetrical Towelettes Cleanser is under an active FDA recall as of Jan. 20, 2026. The recall cites CGMP Deviations that could affect product quality. Consumers and healthcare providers should stop using the product immediately and contact ACME United Corporation or a healthcare provider for guidance.

BZK PADS
CGMP Deviations
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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 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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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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Recalled Halloween-themed Skeleton Wax Candle
HIGH
CPSC

Kroger Recalls Skeleton Wax Candles Over Fire Hazard

Kroger recalled Halloween-themed Skeleton Wax Candles on October 30, 2025. The candles contain flammable ornaments that pose fire and burn hazards. Consumers should stop using these candles and return them for a full refund.

Halloween-themed
The candle
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Health & Personal Care
HIGH
FDA DEVICE

Philips Ultrasound X3-1 Transducer Recalled for Labeling Clarification in 2026 (17 Units)

Philips Ultrasound recalled 17 X3-1 ultrasound transducers nationwide in the United States. The recall is to provide clarification and labeling to define the useful life of transducers in the field. Healthcare providers and patients should stop using the affected devices immediately and await further manufacturer instructions.

Philips Ultrasound
To provide
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Health & Personal Care
LOW
FDA DEVICE

Philips 3D6-2 Ultrasound Transducer Recalled for Labeling Clarification (17 Units, 2025)

Philips recalled 17 units of the 3D6-2 Ultrasound Transducer distributed nationwide to healthcare facilities in the United States. The recall seeks to clarify labeling defining the transducer’s useful life. Clinicians and facilities should stop using the device immediately and follow Philips recall instructions.

Philips Ultrasound
To provide
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Tag Statistics

Total Recalls
37

Related Tags

immediate actionstop use immediatelyreplacement availablefda regulatedcpsc regulatedelectrical hazardsuffocation riskinfant productadult productnhtsa regulatedreturn for refundpoisoning risk