Health & Personal Care Recalls

1,882 product recalls found in this category. Browse through all safety alerts and stay informed.

High Activity Category

This category has a significant number of recalls. Please check regularly for updates.

Health & Personal Care
HIGH
FDA DRUG

Walgreens Saline Nasal Spray With Xylitol Recalled for Microbial Contamination (41,328 Bottles, 2025

Walgreens Saline Nasal Spray With Xylitol, distributed by Walgreens Co., is recalled nationwide. The product was found with microbial contamination, specifically Pseudomonas lactis, in a non-sterile formulation. Consumers should stop using the product immediately and contact Medical Products Laboratories, Inc. for guidance or consult a clinician.

Medical Products Laboratories
Microbial contamination
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Resection Sheath Recalled Due to Breaking Ceramic Tip

Olympus Corporation of the Americas recalled 3,484 units of the Resection Sheath Model No. A22041A on November 11, 2025. Reports indicate the ceramic tip of the device may break during use, posing a serious hazard to patients. Healthcare providers and patients must stop using the device immediately and follow recall instructions.

Olympus Corporation of the Americas
Complaints of
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Sheath Recalled Over Risk of Ceramic Tip Breakage

Olympus recalled 94 units of its 10 Fr. endoscopic sheath on November 11, 2025, due to complaints of the ceramic tip breaking. The defect poses a high risk for patients undergoing urological procedures. Healthcare providers and patients must stop using the device immediately.

Olympus Corporation of the Americas
Complaints of
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Inner Sheath Recalled Due to Ceramic Tip Breakage Hazard

Olympus Corporation of the Americas recalled the Inner Sheath Model No. A2641 on November 11, 2025. The recall follows complaints of the ceramic tip breaking, posing a high risk of injury to patients. Healthcare providers and patients should stop using the device immediately and follow recall instructions.

Olympus Corporation of the Americas
Complaints of
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Resection Sheath Recalled Due to Breakage Risk

Olympus Corporation recalled 29 units of its Resection Sheath on November 11, 2025. The recall affects model numbers A22014A and A22014T due to complaints of the ceramic tip breaking. The company advises immediate cessation of use and adherence to recall instructions.

Olympus Corporation of the Americas
Complaints of
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Resection Sheath Recalled Due to Breaking Tips

Olympus Corporation of the Americas recalled 1,676 units of Resection Sheath Model No. A22042A on November 11, 2025. Complaints indicated the ceramic tip of the sheath could break during use, posing a hazard to patients. Healthcare providers and patients must stop using the device immediately and follow recall instructions.

Olympus Corporation of the Americas
Complaints of
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Resection Sheath Recalled Due to Breakage Hazard

Olympus Corporation of the Americas recalled the Resection Sheath Model A2666T on November 11, 2025. The recall follows reports of the ceramic tip breaking, posing a high hazard for patients. Healthcare providers and patients should stop using the device immediately.

Olympus Corporation of the Americas
Complaints of
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Recalls Endoscopic Sheath Due to Breakage Risk

Olympus Corporation of the Americas recalled 91 units of the Inner Sheath Model No. A4741 on November 11, 2025. The recall follows reports of the ceramic tip breaking, posing a high risk to patients. Healthcare providers and patients must stop using the device immediately and follow recall instructions.

Olympus Corporation of the Americas
Complaints of
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Resection Sheath Recalled Due to Ceramic Tip Breakage

Olympus Corporation recalled 899 units of the Resection Sheath Model No. A42011A on November 11, 2025. Complaints indicate that the ceramic tip may break during use, posing a high risk to patients. Healthcare providers and patients must stop using the device immediately.

Olympus Corporation of the Americas
Complaints of
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Resection Sheath Recalled Due to Ceramic Tip Breaking

Olympus Corporation of the Americas recalled 1,634 units of the A22042T Resection Sheath on November 11, 2025. The recall follows complaints of the ceramic tip breaking, posing a high risk to patients. Healthcare providers and patients must stop using the device immediately.

Olympus Corporation of the Americas
Complaints of
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Resection Sheath Recalled Due to Breaking Hazard

Olympus Corporation of the Americas recalled 207 units of its Resection Sheath, Model No. A22043T, on November 11, 2025. The recall follows reports of the ceramic tip breaking, posing a serious hazard. Patients and healthcare providers must stop using the device immediately.

Olympus Corporation of the Americas
Complaints of
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Resection Sheath Recalled Due to Breaking Tip Hazard

Olympus Corporation of the Americas recalled 2,626 units of its Resection Sheath on November 11, 2025. The ceramic tip of the sheath may break during use, posing a high risk to patients. Healthcare providers and patients must stop using the device immediately.

Olympus Corporation of the Americas
Complaints of
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Resection Sheath Recalled Due to Ceramic Tip Hazard

Olympus Corporation of the Americas recalled 118 units of its 28 Fr. resection sheath on November 11, 2025. The recall follows reports of the ceramic tip breaking, posing a risk of injury. Healthcare providers and patients must stop using the device immediately.

Olympus Corporation of the Americas
Complaints of
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Inner Sheath Recalled Over Breaking Ceramic Tip Hazard

Olympus Corporation of the Americas recalled 437 units of the Inner Sheath, Model No. WA22017A, on November 11, 2025. The recall follows complaints of the ceramic tip breaking during use, posing a significant risk to patients. Healthcare providers and patients should cease use immediately and follow the manufacturer’s instructions.

Olympus Corporation of the Americas
Complaints of
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Recalls Inner Sheath Due to Breaking Ceramic Tip Hazard

Olympus Corporation of the Americas recalled 1,141 units of the Inner Sheath, Model No. WA22017T, on November 11, 2025. The recall follows reports of the ceramic tip breaking, posing a high risk to patients. Healthcare providers and patients must stop using the device immediately and follow the manufacturer’s instructions.

Olympus Corporation of the Americas
Complaints of
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Resection Inner Sheath Recalled Due to Breakage Risk

Olympus Corporation of the Americas recalled 6,949 units of its Resection Inner Sheath on November 11, 2025, after reports of the ceramic tip breaking. This device, used in urologic applications, poses a high hazard risk. Healthcare providers and patients should stop using the device immediately.

Olympus Corporation of the Americas
Complaints of
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Recalled Endoscopic Sheath Due to Breakage Risk

Olympus Corporation of the Americas recalled the Inner Sheath Model No. A2660 on November 11, 2025. Complaints of the ceramic tip breaking prompted the recall of nine units distributed nationwide. Patients and healthcare providers must stop using the device immediately.

Olympus Corporation of the Americas
Complaints of
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Inner Sheath Recalled Due to Ceramic Tip Risk

Olympus recalled its Inner Sheath, Model No. A2642, on November 11, 2025, due to safety complaints. Users reported the ceramic tip of the resection sheath breaking during use. This recall affects urological applications and poses a high risk to patients.

Olympus Corporation of the Americas
Complaints of
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Resection Sheath Recalled Due to Breakage Risk

Olympus Corporation recalled the Resection Sheath, Model No. A2666, on November 11, 2025, following complaints of the ceramic tip breaking. The recall affects one unit distributed nationwide in the U.S. Healthcare providers and patients must stop using the device immediately.

Olympus Corporation of the Americas
Complaints of
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Health & Personal Care
HIGH
FDA DRUG

Dr. Reddy's Labs Recalls Varenicline Tablets Over Potency Issues

Dr. Reddy's Laboratories recalled 4,800 bottles of Varenicline tablets on November 11, 2025, due to sub potent drug levels. The affected lot failed stability tests, posing potential health risks to users. Consumers should stop using the product immediately and consult healthcare providers.

VARENICLINE TARTRATE
Sub potent
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Category Statistics

Total Recalls
1,882
Pages
95