holiday product Recalls

153 recalls tagged with “holiday product”.

Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter Recalls 160 DxC 500i Modules and DxI 9000 Analyzers in 2025 Recall

Beckman Coulter recalls 160 DxC 500i Clinical Analyzer Modules and the DxI 9000 Access Immunoassay Analyzer worldwide after a software anomaly could misapply manual dilution factors. The defect affects samples already in progress using the same Sample ID. Stop using the devices immediately and follow the recall instructions. Beckman Coulter will provide instructions via the recall process.

Beckman Coulter
Beckman Coulter
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Food & Beverages
HIGH
FDA FOOD

Black Sheep Egg Company Recall: 288,900 Dozen Free Range Grade AA Eggs Over Salmonella Risk

Black Sheep Egg Company is recalling 288,900 dozen Free Range Grade AA Large Brown Eggs sold at retail and wholesale locations in Arkansas and Missouri, with broker distribution in Mississippi, Texas, California and Indiana. The recall cites potential Salmonella contamination as the hazard. Consumers should not consume these eggs and should contact Black Sheep Egg Company for refund or replacement

Black Sheep Egg Company
Potential Salmonella
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Health & Personal Care
HIGH
FDA DEVICE

HeartSine Pad-Pak Defibrillator Pads Recalled for 1,291,165 Units in 2025

HeartSine Technologies recalled 1,291,165 Pad-Pak defibrillator pads sold nationwide in the United States and worldwide. A defect may allow damage pins to disrupt the mechanical fit and electrical contact. Stop using the pads immediately and follow the manufacturer's recall instructions.

HeartSine Technologies
Due to
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Food & Beverages
HIGH
FDA FOOD

Taproom Gourmet Bulk Fifth Avenue Mix Recalled for No Ingredient Label and Allergens

Taproom Gourmet recalled 3,547 cases of 18lb and 20lb bulk Fifth Avenue Mix sold in six states after undeclared peanuts, almonds, cashew, and soy were found. The recall classifies the hazard as HIGH. Consumers should discard the product or return for refund or replacement via Egress Capital Partners Inc.

Taproom Gourmet
No ingredient
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical PERIFIX FX Epidural Tray Recalled for Lid-Position Issue (21,270 Units)

B Braun Medical recalled 21,270 PERIFIX FX Continuous Epidural Anesthesia Tray units distributed nationwide to hospitals and surgical centers after a lid-position defect was identified in the catheter connector. The defect allows the catheter connector lid to be in the incorrect position. Healthcare facilities and clinicians should stop using the device immediately and follow the manufacturer’s or

B Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DRUG

Glenmark Azelaic Acid Gel Recall Affects 13,824 Tubes Sold Nationwide in 2025

Glenmark Pharmaceuticals Inc. USA recalls 13,824 tubes of azelaic acid gel 15% after CGMP deviations prompted gritty texture complaints. The recall covers nationwide distribution in the United States. Consumers should stop using the product and contact Glenmark for guidance.

Glenmark Pharmaceuticals
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DEVICE

GE HealthCare Millenium MPR Gamma Camera Recalled for 292 Units Worldwide in 2025

GE HealthCare recalled 292 Millenium MPR dual-head gamma cameras worldwide after discovering some units past End of Guaranteed Service may have been transported without adequate detector support. This can place excessive stress on detector mounting and could result in a detector fall with life-threatening injury. Healthcare facilities should stop using the devices immediately and follow recall PIN

GE HealthCare
GE HealthCare
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Health & Personal Care
HIGH
FDA DEVICE

Boston Scientific Recall: Preconnect with TENACIO Pump with InhibiZone Affects 172 Units Worldwide

Boston Scientific recalled 172 units of the CXR Preconnect with TENACIO Pump with InhibiZone worldwide. The recall was initiated on 2025-09-11 and remains active as of 2025-10-22. The devices can experience inflation and/or deflation performance issues. Healthcare providers should stop using the devices and follow manufacturer instructions for recall remediation.

Boston Scientific
The potential
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Food & Beverages
HIGH
FDA FOOD

Harris Teeter recalls Asiago Texas Toast for undeclared milk in 295 units

Harris Teeter recalls 295 units of Asiago Texas Toast distributed in eight states after discovering undeclared milk. The allergen milk was not listed in the ingredient statement. Consumers with milk allergies should avoid the product and seek refunds or replacements.

Harris Teeter
Undeclared Milk.
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Food & Beverages
HIGH
FDA FOOD

Gina Marie Bakery Cookies Recalled for Undeclared Red 40 and Yellow 6

Gina Marie Bakery LLC recalls Vanilla with Apricot Jam Cookies due to undeclared artificial colorings Red 40 and Yellow 6. The recall, initiated by the state of Connecticut and notified to the FDA, involves 172 cases at 20 containers per case. FDA-listed recall status is ACTIVE with no reported incidents yet.

Gina Marie Bakery
Undeclared Red
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Food & Beverages
HIGH
FDA FOOD

Gina Marie Bakery Biscotti Recalled for Undeclared Red 40

Gina Marie Bakery LLC recalled 172 cases of Toasted Almond & Cherry Biscotti after the FDA flagged undeclared Red 40. The recall is classified as high hazard. Consumers should avoid the product and contact the company for refunds or replacements.

Gina Marie Bakery
Undeclared Red
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Health & Personal Care
HIGH
FDA DEVICE

Draeger Atlan A350 Anesthesia Workstations Recalled for Ventilator Failures in 2025

Drӕager recalled 530 Atlan A350 anesthesia workstations imported from Draegerwerk AG and Co. KGaA and distributed to 25 U.S. states and more than 30 countries. The device can experience a piston ventilator failure before use or fail to ventilate during use. Hospitals should stop using affected units immediately and follow Draeger recall instructions.

Draeger
The device
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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
153

Related Tags

fda regulatedstop use immediatelyimmediate actionreplacement availablecpsc regulatedelectronicinfant productadult productpoisoning riskelectrical hazardworkplacereturn for refund
    holiday product Recalls | RecallRadar