All Product Recalls

Browse through 2,959 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

Health & Personal Care
HIGH
FDA DEVICE

Siemens Healthcare Diagnostics Recalls 4,885 Atellica CH Urine Albumin Tests for False Low Results (

Siemens Healthcare Diagnostics recalled 4,885 Atellica CH Urine Albumin tests in 2026 after detecting falsely depressed results. The manufacturer notes that any urine albumin concentration above 40.0 mg/dL may report values from 6.2 to 40.0 mg/dL. Stop using the device immediately and follow the recall instructions.

Siemens Healthcare Diagnostics
Falsely depressed
Read more
Food & Beverages
HIGH
FDA FOOD

Frederik's by Meijer Focaccia Bread Recalled for Metal Fragments (2026)

Frederik's by Meijer Slow-Roasted Tomato & Parmesan Focaccia Bread recalled after metal fragments were found in 23,459 cases. The recalls spans Frederik's by Meijer, Fresh & Simple, HT Traders and Trader Joe's focaccia products. The metal fragments were traced to roasted tomatoes from an ingredient supplier. Stop using the product and contact the supplier for refunds or replacements.

Bakkavor
Metal fragments
Read more
Food & Beverages
HIGH
FDA FOOD

Tradin Organics Recalls Chia Seeds Due to Salmonella Risk

Tradin Organics USA, LLC recalled 54,680 pounds of Organic Chia Seed Black on January 18, 2026. The recall follows potential contamination with Salmonella, posing serious health risks. Consumers should not consume this product and seek refunds or replacements immediately.

Tradin Organics USA
Potential contamination
Read more
Food & Beverages
HIGH
FDA FOOD

Palmetto Gourmet Foods Vegetarian Chicken Flavor Ramen Recalled for Yellow #5 (5,664,960 Units, 2026

Palmetto Gourmet Foods recalled 5,664,960 three-ounce packages of Vegetarian Chicken Flavor Ramen sold at multiple retailers nationwide after undeclared Yellow #5 was detected. The recall covers products with a Best By Date before 01/15/2027. Consumers should not eat this product and should contact Palmetto Gourmet Foods for refund or replacement information by mail.

Palmetto Gourmet Foods
Product contains
Read more
Health & Personal Care
HIGH
FDA DEVICE

Olympus Insufflation Unit Recalled Due to Overpressure Hazard

Olympus Corporation recalled 744 High Flow Insufflation Units on January 16, 2026. A software algorithm issue may lead to overpressure events during use. Patients and healthcare providers must stop using the device immediately.

Olympus Corporation of the Americas
Issue with
Read more
Health & Personal Care
HIGH
FDA DEVICE

Integra LifeSciences Recalls Medical Dressing Due to Sterility Risk

Integra LifeSciences Corp. recalled 55,276 units of MEDIHONEY Calcium Alginate with Active Leptospermum Honey on January 16, 2026. The recall cites potential packaging failures that may compromise sterility. Affected products include model numbers 31012, 31022, and 31045.

Integra LifeSciences Corp.
Potential packaging
Read more
Food & Beverages
HIGH
FDA FOOD

Bader Enterprises Recalls Premium Food Jordan Almonds in 2.0 oz & 3.5 oz Packaging (2026 Recall)

Bader Enterprises recalls 60 pounds of Premium Food Jordan Almonds sold in New Jersey and New York. The product contains undeclared wheat and blue color additives. Consumers who purchased the product should not consume it. Contact Bader Enterprises for refund or replacement information via two or more notification methods.

Bader Enterprises
Contains undeclared
Read more
Health & Personal Care
HIGH
FDA DEVICE

GE Healthcare Centricity Universal Viewer ZFP Recall 250 Units Worldwide in 2026

GE Healthcare recalled 250 Centricity Universal Viewer Zero Footprint Client units distributed worldwide after finding a risk that patient information may not match displayed images in certain workflows. The issue affects ZFP v6.0 SP11.6, SP11.6.0.1 and SP11.6.1 when Patient Timeline is installed. Hospitals should stop using affected units and await instructions from GE Healthcare.

GE Healthcare
Under certain
Read more
Health & Personal Care
HIGH
FDA DRUG

Specialty Process Labs Issues Recall for Subpotent Thyroid Drug

Specialty Process Labs recalled 58 grams of Thyroid, USP due to subpotency. The recall affects products distributed nationwide. Consumers should stop using the drug immediately and contact their healthcare provider.

Specialty Process Labs
Subpotent Drug
Read more
Health & Personal Care
HIGH
FDA DEVICE

Integra LifeSciences Recalls MediHoney Gel for Packaging Issues

Integra LifeSciences Corp. recalled 49,367 units of MediHoney Gel on January 16, 2026. The recall follows potential packaging failures that may compromise the sterile barrier. Affected products include model numbers 31805 and 31815, distributed worldwide.

Integra LifeSciences Corp.
Potential packaging
Read more
Health & Personal Care
HIGH
FDA DEVICE

Olympus Insufflation Unit Recalled Over Software Malfunction

Olympus Corporation recalled 485 units of the High Flow Insufflation Unit, Model UHI-3, on January 16, 2026. The recall follows reports of a software algorithm issue that may cause overpressure events. Patients and healthcare providers must stop using the device immediately.

Olympus Corporation of the Americas
Issue with
Read more
Health & Personal Care
HIGH
FDA DEVICE

Olympus Insufflation Unit Recalled Due to Software Hazard

Olympus Corporation recalled 18 High Flow Insufflation Units on January 16, 2026, due to a software issue that can cause overpressure events. The recall affects model number UHI, which is used for laparoscopic procedures. Healthcare providers and patients must stop using the device immediately.

Olympus Corporation of the Americas
Issue with
Read more
Health & Personal Care
HIGH
FDA DEVICE

CVS Wound Care Device Recalled Due to Sterile Barrier Breach

CVS recalled 2,906 units of its wound care device on January 16, 2026. The recall stems from potential packaging failures that may compromise sterility. Affected products include model number CVS405406, distributed across multiple states and internationally.

Integra LifeSciences Corp.
Potential packaging
Read more
Health & Personal Care
HIGH
FDA DEVICE

Encore Medical Recalls Shoulder Prosthesis Over Labeling Error

Encore Medical, LP recalled 20 shoulder prosthesis implants on January 15, 2026. Incorrect labeling on the RSP Standard Humeral Socket Insert poses a high hazard risk. Affected products were distributed nationwide across multiple states.

Encore Medical, LP
Knee and
Read more
Health & Personal Care
HIGH
FDA DEVICE

Encore Medical Recalled Humeral Socket Insert Over Labeling Issues

Encore Medical, LP recalled 20 units of its RSP Humeral Socket Insert on January 15, 2026. The recall stems from incorrect labeling on knee and humeral socket implants. Patients and healthcare providers should stop using the device immediately.

Encore Medical, LP
Knee and
Read more
Health & Personal Care
HIGH
FDA DEVICE

Aesculap MINOP TROCAR 150MM Recall for 126 Units in 2026

Aesculap recalls 126 MINOP TROCAR 150MM devices distributed nationwide to U.S. hospitals and clinics after regulators flagged a shaft length issue. The shaft may be longer than specified, potentially harming tissue during procedures. Healthcare facilities should stop using the devices and follow manufacturer recall instructions immediately.

Aesculap
There is
Read more
Previous
12345...148
Next
Advertisement