holiday product Recalls

153 recalls tagged with “holiday product”.

Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Anesthesia IV Set Recalled for Backflow Risk (10,536 Units) 2025

B. Braun Medical recalled 10,536 Anesthesia IV Sets sold through multiple retailers worldwide after a potential backflow from piggyback to primary IV lines and occlusion. The devices are used with Infusomat Space Large Volume Pumps, Outlook Pumps, and Vista Basic Pumps. Hospitals and healthcare providers should stop using the device immediately and follow the manufacturer’s recall instructions.

B. Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical Inc. Recalls 28,344 IV Administration Sets Linked to Backflow and Occlusion Risks (Z

B Braun Medical Inc. recalls 28,344 IV administration sets used with several BBMI infusion pumps after reports of backflow and occlusion risks. The recall covers a catalog number 470179 device distributed worldwide including the U.S., Canada, Germany, Guatemala and Singapore. The issue involves potential backflow from secondary IV containers into primary containers and the inability to prime the管.

BBraun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical IV Administration Set Recall: 5,100 Units Distributed Worldwide Over Backflow and Oc

B Braun Medical Inc. recalls 5,100 IV administration sets distributed worldwide, including the US, Canada, Germany, Guatemala and Singapore. The recall cites backflow of medication from piggyback containers into primary IV containers and an occlusion that prevents priming. Patients should stop use immediately and follow recall instructions.

BB Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical IV Administration Sets Recall Over Backflow and Occlusion Risk (2025)

B Braun Medical Inc. recalls 190,625 IV administration sets worldwide, including US and Canada, for risk of backflow from secondary to primary IV containers and occlusion that prevents priming. The recall affects BBMI’s Infusomat Space, Outlook Pump, and Vista Basic Pump compatible sets. Stop-use immediately and follow recall instructions.

BBraun Medical
Potential for
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Health & Personal Care
HIGH
FDA FOOD

Avion Pharmaceuticals Prenate Chewable Prenatal Vitamin Recalled for Undeclared Soy (804 Bottles, 5

Avion Pharmaceuticals recalled 804 bottles of Prenate Chewable prenatal vitamins shipped to 17 states after tests found undeclared soy and a boron labeling error. The product lists boron as 250 mg per serving instead of 250 mcg per serving. Consumers should not take the product and should contact Avion Pharmaceuticals for refund or replacement.

Avion Pharmaceuticals
Undeclared Soy.
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Recalled Sauna Model Tylö Halmstad 2
MEDIUM
CPSC

Sauna360 Recalls Tylö Halmstad and Kiruna Hybrid Saunas Over Fall Hazard

Sauna360 recalls Tylö Halmstad and Kiruna Hybrid saunas sold by Sauna360 distributors nationwide from July 2024 through December 2024 for between $6,000 and $12,000. The recall targets bench seating that can collapse, creating a fall hazard. Stop using the benches immediately and contact Sauna360 for a free repair.

Sauna360
The saunas
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Recalled Bealife 5-Drawer Dresser (front)
HIGH
CPSC

Bealife 5-Drawer Dressers Recalled for Tip-Over Hazard in 2025

Bealife recalled its 5-Drawer Dressers on Oct. 23, 2025. The dressers are white and measure 32 inches high, 28 inches wide, and 16 inches deep. The model AP23-W is printed on packaging but not on the dresser itself. Consumers should stop using unanchored dressers and seek a full refund.

Bealife
The recalled
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Health & Personal Care
HIGH
FDA DRUG

CA Botana Doctor D. Schwab Shimmery Sun Lotion Sunscreen Recall for CGMP Deviations (2025)

CA Botana International recalled 805 tubes of Doctor D. Schwab Shimmery Sun Lotion Sunscreen SPF 30 after CGMP deviations were identified. The recall covers tubes sold in California, Colorado, Florida, Puerto Rico, and Washington. Consumers should stop using the product immediately and contact the company for guidance.

Doctor D. Schwab
CGMP Deviations
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Health & Personal Care
HIGH
FDA DRUG

STAQ Pharma Hydromorphone HCl PF 10mg/50mL IV Injection Recall for Labeling Errors (2025)

STAQ Pharma’s Hydromorphone HCl PF 10mg/50mL IV injection recall affects nationwide distribution in the United States. The recall cites labeling errors involving incorrect or missing lot and expiration dates. Healthcare providers and patients must stop using the product and follow guidance from STAQ Pharma or their clinician.

STAQ Pharma
Labeling: Incorrect
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Recalled YGJT Baby Lounger
HIGH
CPSC

YGJT Baby Loungers Recalled on SHEIN for Entrapment and Fall Risk (2025)

YGJT recalled baby loungers sold on SHEIN by YGJT Local Warehouse from June 2025 through August 2025 for $18-$21. The recall cites a safety violation that allows infants to be trapped or fall due to low sides, wide openings at the foot, and no stand. Consumers should stop using the loungers immediately and request a full refund by emailing YGJTrecall@outlook.com.

YGJT
The recalled
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Food & Beverages
HIGH
FDA FOOD

Great Lakes Cheese Co Italian Style Shredded Cheese Blend Recalled for Metal Fragments (15,490 cases

Great Lakes Cheese Co is recalling 15,490 cases of Italian Style Shredded Cheese Blend sold at multiple retailers nationwide after reports of potential metal fragments. The hazard stems from metal fragments in the cheese sourced from supplier raw material. Consumers should not eat these products and should contact Great Lakes Cheese Co for refunds or replacements.

Great Lakes Cheese
Potential metal
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Recalled Evermore Surprise Egg – Yellow Wrap
HIGH
CPSC

In Motion Design Recalls Evermore Surprise Eggs for Lead Hazard

In Motion Design recalled Evermore Surprise Eggs due to lead content above federal limits. The recalled eggs were sold with yellow, pink or green wrap and include a gold egg containing seven toys, including a toy airplane. Consumers should stop using the product and return it for a full refund.

In Motion Design
The toy
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Health & Personal Care
HIGH
FDA DRUG

Medline 222,800 Alcohol Prep Pads Recalled for Subpotent Drug (2025)

Medline Industries recalled 222,800 alcohol prep pads nationwide on Sept. 29, 2025 due to subpotent potency. The pads are 2-ply, 70% isopropyl alcohol. Stop using immediately and contact Medline or your healthcare provider for guidance.

Medline Industries
Subpotent Drug
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Food & Beverages
HIGH
FDA FOOD

Albertsons Store-Made Grilled Chicken & Basil Pasta Extra Large Recalled for Listeria (2025)

Albertsons Companies is recalling store-made Grilled Chicken & Basil Pasta Extra Large sold under Carrs-Safeway, Eagle and Safeway banners. The product contains a bowtie pasta ingredient recalled for Listeria monocytogenes contamination. It was distributed in AK, AR, AZ, CA, CO, HI, LA, NE, NM, NV, OK, SD, TX, UT and WY. Stop using the product and contact Albertsons for refund or replacement.

Albertsons
Listeria monocytogenes.
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Health & Personal Care
HIGH
FDA DRUG

Aloe Up Sunscreen Lotion SPF 30 Recalled for Microbial Testing Failure in 2025 (11,386 Tubes)

Aloe Up recalled 11,386 tubes of Aloe Up Sport Performance Sunscreen Lotion SPF 30 sold nationwide in the United States. The recall cites cGMP deviations after the product failed total aerobic microbial count testing. Consumers should stop using the product and follow guidance from SV Labs Prescott Corporation or a healthcare provider.

Aloe Up
cGMP deviations:
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Tag Statistics

Total Recalls
153

Related Tags

immediate actionstop use immediatelyreplacement availablereturn for refundcpsc regulatedfda regulatedworkplaceplasticmetalback to schoolinfant productadult product
    holiday product Recalls | RecallRadar