stop use immediately Recalls

2,154 recalls tagged with “stop use immediately”.

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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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

Insulet Omnipod 5 iOS App Recall Affects 174,013 Units in 2025

Insulet recalled 174,013 Omnipod 5 iOS app software units distributed nationwide in the United States. The recall cites a magnifying feature bug that can duplicate a single-digit entry. This could lead to bolus insulin dosing errors and hypoglycemia. Stop using the app immediately and follow recall instructions from Insulet or your healthcare provider.

Insulet
The failure
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Recalls EVIS EXERA Bronchoscope Over Safety Concerns

Olympus Corporation of the Americas recalled 262 EVIS EXERA bronchoscopes on September 11, 2025. The recall addresses safety issues related to the use of bronchoscopes with laser and coagulation equipment. Healthcare providers and patients must stop using the devices immediately for safety reasons.

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

Olympus BF-P60 Bronchoscope Recall Affects 6,450 Units in 2025 for IFU Updates

Olympus recalled 6,450 BF-P60 bronchofiberscopes worldwide after updated instructions clarify safe use with laser, argon plasma coagulation and high-frequency therapy devices. The recall covers 1,007 US units and 5,443 units outside the US. Healthcare providers should stop using the device immediately and follow manufacturer instructions. Contact Olympus Corporation of the Americas for guidance.

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

Boston Scientific TENACIO Pump Recall 2025 for Inflation Deflation Issues

Boston Scientific recalled the TENACIO Pump without InhibiZone (UPN 72404420) worldwide, including the US and Canada. The device may experience inflation and/or deflation performance issues. Patients and healthcare providers should stop using the device immediately and follow the manufacturer's recall instructions.

Boston Scientific
The potential
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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

Olympus BF-P190 Bronchoscope Recall Updated for 2025 IFU Guidance

Olympus recalls 3,046 BF-P190 bronchovideoscopes sold nationwide in the US and 2,414 overseas. The recall centers on updated IFU guidance to clarify safe use with laser, argon plasma coagulation, and high-frequency therapy equipment. Clinicians and facilities should stop using the device immediately and follow Olympus recall instructions.

Olympus
Additional IFU
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Food & Beverages
HIGH
FDA FOOD

Tropicana Brands Group Recalls 1,599 Cases of Dole Apple Juice 15.2 oz PET (2025)

Tropicana Brands Group recalled 1,599 cases of Dole Apple Juice in 15.2 oz PET bottles. The recall covers products distributed to 11 states. A manufacturing process deviation may cause spoilage or microbial contamination and affect shelf stability. Consumers should not consume the product and should contact Tropicana Brands Group for refund or replacement by telephone.

Tropicana Brands Group
A manufacturing
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Health & Personal Care
HIGH
FDA DEVICE

Olympus BF-TE2 Bronchofiberscope Recall for IFU Updates in 2025

Olympus Corporation of the Americas recalls the BF-TE2 bronchofiberscope distributed nationwide in the United States. The recall updates the Instructions for Use 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 instructions.

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

Olympus EVIS EXERA II BF-1T180 Bronchovideoscope Recall for IFU Update — 5,247 Units (2025)

Olympus Corporation of the Americas recalled 1,473 US units and 3,774 non-US units of the EVIS EXERA II bronchovideoscope BF-1T180. The recall concerns updated instructions for safe use with laser, argon plasma coagulation, and high-frequency therapy equipment. Stop using the device immediately and follow manufacturer instructions.

Olympus
Additional IFU
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Health & Personal Care
HIGH
FDA DEVICE

Olympus EVIS EXERA III BF-1TH190 Bronchoscope Recall 8,587 Units in 2025

Olympus Corporation of the Americas recalls 8,587 bronchovideoscope units worldwide, including 4,297 in the US and 4,290 outside. The recall centers on updated IFU language for safe use with laser, argon plasma coagulation and high-frequency therapy equipment. Stop using the device immediately and follow manufacturer instructions for remediation.

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

Ethicon Endo-Surgery ECHELON 80 mm Blue Linear Cutter Recalled for Unsterilized Shipment (3 Units, 3

Ethicon Endo-Surgery recalled 3 ECHELON Linear Cutter Reload 80 mm Blue devices, Product Number GLC80, distributed internationally to the United Arab Emirates, after they were shipped unsterilized. The devices were shipped unsterilized, creating a potential infection risk. Healthcare providers should stop using the device immediately and await instructions from Ethicon Endo-Surgery.

Ethicon Endo-Surgery
The devices
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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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Health & Personal Care
HIGH
FDA DEVICE

Olympus BF-H1100 Bronchovideoscope Recall 1,867 Units Overseas in 2025

Olympus BF-H1100 bronchovideoscopes sold nationwide in the US were recalled. The recall updates the IFU 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 instructions.

Olympus
Additional IFU
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Health & Personal Care
HIGH
FDA DEVICE

Olympus BF-1TQ170 Bronchoscope Recall Expanded for IFU Clarifications

Olympus Corporation of the Americas recalls the BRONCHOVIDEOSCOPE BF-1TQ170. The recall is active with 2,092 units in the outside US market and no US units affected. The action seeks updated instructions for safe use with laser and high-frequency therapy equipment. Healthcare providers should stop use and follow manufacturer recall instructions.

Olympus Corporation of the Americas
Additional IFU
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Tag Statistics

Total Recalls
2,154

Related Tags

electrical hazardsuffocation riskinfant productadult productchildren productfederal law violationcpsc regulatedimmediate actionreturn for refundreplacement availablenhtsa regulatedchemical hazard