All Product Recalls

Browse through 2,970 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

Health & Personal Care
HIGH
FDA DEVICE

Medline Excelsior Medical 0.9% Saline Flush Syringes Recalled Over Concentration Deviation (8.27M)

Medline Recall: Excelsior Medical 0.9% Sodium Chloride Injection, USP, 10 mL fill prefilled saline flush syringes EMZ111240 is being recalled. The notice covers 8,267,150 syringes distributed across the United States and Canada. The risk is a concentration deviation of sodium chloride. Healthcare facilities should stop using the product and follow recall instructions. See the FDA recall page for完整

Medline Industries, LP
Medline has
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Health & Personal Care
HIGH
FDA DEVICE

Olympus BF-1T60 Bronchofiberscope Recall for IFU Updates (2025)

Olympus recalled 3,216 BF-1T60 bronchofiberscopes distributed nationwide and internationally after updating instructions for safe use with laser, argon plasma coagulation and high-frequency therapy equipment. The recall updates guidance to reduce risk during advanced energy-device procedures. Clinicians and facilities should stop using the devices and follow manufacturer instructions for recall.

Olympus Corporation of the Americas
Additional IFU
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Food & Beverages
HIGH
FDA FOOD

Harris Teeter Cinnamon Texas Toast Recalled for Undeclared Milk (83 Units) 2025

Harris Teeter recalled 83 units of Cinnamon Texas Toast sold across DC, DE, FL, GA, MD, NC, SC and VA after discovering undeclared milk. The ingredient statement did not list milk despite ingredients including cheese and butter. Consumers should not consume these products and should contact Harris Teeter for a refund or replacement.

Harris Teeter
Undeclared Milk.
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Health & Personal Care
HIGH
FDA DEVICE

Olympus EVIS EXERA III BF-Q190 Bronchovideoscope Recall Expands in 2025 for IFU Updates

Olympus Corporation of the Americas recalled 916 BF-Q190 bronchovideoscopes in the United States and 1,402 outside the US. The recall seeks to clarify safe use with laser, argon plasma coagulation and high-frequency therapy equipment. Stop using the device immediately and follow the manufacturer’s recall guidance.

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

Boston Scientific LGX Preconnect with TENACIO Pump Recalled for Inflation/Deflation Issues (2025)

Boston Scientific recalled two UPN configurations of the LGX Preconnect with TENACIO Pump without InhibiZone due to potential inflation and deflation performance issues. The devices were distributed worldwide, including the US and Canada. Healthcare providers are instructed to stop use and follow manufacturer recall instructions.

Boston Scientific
The potential
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Health & Personal Care
HIGH
FDA DEVICE

CareFusion 303 BD Alaris Infusion Sets Recalled for Flow, Bolus Accuracy Issues (2025)

CareFusion 303 BD Alaris infusion pump modules and compatible infusion sets are recalled nationwide in the U.S. and multiple international markets. The recall covers reference numbers including C24101E and 10015414 and related SmartSite components. The defect may cause flow rate and bolus accuracy deviations, and incorrect occlusion timing. Stop using the device and follow recall instructions from

CareFusion
Infusion pump
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Food & Beverages
HIGH
FDA FOOD

Gina Marie Bakery Recalls 3,440 Vanilla Cookies with Raspberry Peach Jam for Red 3 and Blue 1 (2025)

Gina Marie Bakery LLC recalled 3,440 Vanilla Cookies with Raspberry Peach Jam distributed in Connecticut after undeclared Red 3 and Blue 1 were detected. The recall was announced by state authorities and shared with FDA. Consumers should not eat the product and should contact Gina Marie Bakery LLC for refunds or replacements.

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

Abbott TactiFlex Sensor Ablation Catheter Recall 2025 Affects 1,958 Units

Abbott recalled 1,958 TactiFlex Sensor Enabled Ablation Catheters worldwide. A limited number of tip detachment events occurred during catheter removal from packaging. Patients and healthcare providers should stop using the device immediately and follow Abbott's recall instructions.

Abbott
Abbott has
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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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Food & Beverages
HIGH
FDA FOOD

Gina Marie Bakery Italian Sesame Cookies Recalled for Undeclared Sesame and Food Colorings (2025)

Gina Marie Bakery LLC recalled 172 cases of Italian Sesame Cookies after discovering undeclared sesame and artificial colorings. The recall began with CT state actions and was notified to FDA on 09/10/2025 with customer notification on 09/11/2025. Consumers should not eat these cookies and should seek refunds or replacements.

Gina Marie Bakery
Undeclared Sesame,
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Health & Personal Care
HIGH
FDA DEVICE

Biomet Juggerknot Mini Soft Anchors 912080 Recall 40 Units Nationwide 2025

Biomet recalled 40 Juggerknot Mini Soft Anchors, model 912080, distributed nationwide in the United States. The outer carton label lists JuggerKnot 1.0mm Mini devices, but the cartons contain JuggerKnot 1.4mm Short devices. Patients and clinicians should stop using the device and follow the recall instructions provided by Biomet.

Biomet
The outer
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Health & Personal Care
HIGH
FDA DEVICE

MedicalCommunications GmbH Recalls 474 Ashvins HEYEX 2 / HEYEX PACS Software Units (2025)

MedicalCommunications GmbH recalled 474 Ashvins HEYEX 2 / HEYEX PACS software units distributed nationwide in the United States. The affected software versions range from 2.6.0 (Build 2088) to 2.6.8 (Build 2220). The hazard is that the measured value may be smaller than the actual area, potentially affecting imaging measurements. Stop using the software immediately and follow manufacturer recall‑s

MedicalCommunications
Potential that
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