Official U.S. recalls · explained plainly

Know if it’s recalled — and exactly what to do.

We pull official government recall records and translate each one into plain language: what happened, how serious it is, and the steps to take. No legalese.

Search by meaning, not just keywords — describe the product or the hazard and we’ll find matching recalls even when the official notice uses different words. Brand names and model numbers work too.

Latest recalls

77,052 found

✓ Lower riskMedical device
Olympus Corporation of the Americas recalls Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: THUNDERBEAT 5 mm,35 cm
Olympus recalls Thunderbeat 5mm, 35cm hand instruments due to probe tips breaking. Affected models include TB-0535FCS with catalog number N542:3630. Stop using if you have this instrument.
OlympusNov 25, 2024
✓ Lower riskMedical device
Olympus Corporation of the Americas recalls Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: Thunderbeat, 5MM, 35CM,
Olympus recalls Thunderbeat 5MM, 35CM hand instruments due to probe tip damage or detachment. Affected items have model TB-0535FCS and catalog number N5423810. Stop using if you have these instruments.
OlympusNov 25, 2024
✓ Lower riskMedical device
Olympus Corporation of the Americas recalls Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: THUNDERBEAT 5 mm,20 cm,
Olympus recalls Thunderbeat 5mm,20cm hand instruments due to probe tip damage or detachment. Affected units have model TB-0520FCS and catalog N5424110. Stop using if damaged.
OlympusNov 25, 2024
⚠️ Use cautionMedical device
Spacelabs Healthcare, Inc. recalls Xhibit Telemetry Receiver with Software, Model 96280. Intended to provide monitoring system with patient data.
Spacelabs Healthcare recalls Xhibit Telemetry Receiver software versions 1.4.0 and 1.4.1 that may cause temporary monitoring loss during system shutdowns, risking delayed clinical interventions. Affected units have specific UDI-DI codes.
Spacelabs Healthcare

Know if it’s recalled — and exactly what to do.

Latest recalls

Olympus Corporation of the Americas recalls Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: THUNDERBEAT 5 mm,35 cm

Olympus Corporation of the Americas recalls Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: Thunderbeat, 5MM, 35CM,

Olympus Corporation of the Americas recalls Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: THUNDERBEAT 5 mm,20 cm,

Spacelabs Healthcare, Inc. recalls Xhibit Telemetry Receiver with Software, Model 96280. Intended to provide monitoring system with patient data.

GE Medical Systems, LLC recalls GE Healthcare Optima XR240amx, Mobile Digital Radiographic System, Model Numbers: 1) 5555000-27; 2) 5555000-31; 3)

Olympus Corporation of the Americas recalls Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: Thunderbeat Front-Actuated

Olympus Corporation of the Americas recalls Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: THUNDERBEAT 5 mm,45

Spacelabs Healthcare, Ltd. recalls Eclipse Mini REF 98900 The Eclipse MINI Model 98900 is a portable non-invasive continuous ambulatory ECG patch recorder

Olympus Corporation of the Americas recalls Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: THUNDERBEAT 5 mm,20 cm,

Olympus Corporation of the Americas recalls Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: THUNDERBEAT 5 mm,20 cm,

Angiodynamics, Inc. recalls AURYON LASER SYSTEM 100-120 VAC. Model Number: EXM001. Product Number: EXM-2001-1100

Spacelabs Healthcare, Inc. recalls Xhibit Telemetry Receiver, Model 96280, with Service Manual. Intended to provide monitoring system with patient data.

Olympus Corporation of the Americas recalls Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: THUNDERBEAT 5 mm,45

Olympus Corporation of the Americas recalls Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: THUNDERBEAT 5 mm, 35 cm,

Olympus Corporation of the Americas recalls Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: THUNDERBEAT 5 mm,45

GE Medical Systems, LLC recalls GE Healthcare Optima XR200amx, Mobile Digital Radiographic System, Model Numbers: 1) 5555000-3; 2) 5555000-4: 3) A0659MB

GE Medical Systems, LLC recalls GE Healthcare Optima XR220amx, Mobile Digital Radiographic System, Model Numbers: 1) 5555000-12; 2) 5555000-5; 3)

Spacelabs Healthcare, Ltd. recalls Eclipse PRO REF 98700 The Spacelabs model 98700 is a portable non-invasive Holter recorder intended to record the

Olympus Corporation of the Americas recalls Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: THUNDERBEAT 5 mm,35 cm,

Macleods Pharmaceuticals Ltd recalls Olanzapine Tablets, USP 2.5 mg, 30-count bottle, Rx Only, Manufactured for: Macleods Pharma USA, Inc. Princeton, NJ

SE Tampa Inc dba Tampa Food recalls Crab Cheese Rangoon, NET WT: 8 LB, 120 pieces of 30g / 3 Trays per master cardboard boxes, Keep Frozen, packaged in

Adept Medical Ltd recalls Otological Ventilation Tube - Donaldson - Double - Blue Silicone; Product Code: NZ3321-2;

Adept Medical Ltd recalls Otological Ventilation Tube - T-Tube 12mm - Double - Silicone; Product Code: NZ3312-2;

Adept Medical Ltd recalls Otological Ventilation Tube - T-Tube 6mm - Silicone; Product Code: NZ3306/NZ3306-2;

Adept Medical Ltd recalls Otological Ventilation Tube - T-Tube 12mm - Silicone; Product Code: NZ3312;

Adept Medical Ltd recalls Otological Ventilation Tube - T-Tube 9mm - Double - Silicone; Product Code: NZ3309-2;

Adept Medical Ltd recalls Otological Ventilation Tube - Donaldson - Blue Silicone; Product Code: NZ3321;

Adept Medical Ltd recalls Otological Ventilation Tube - T-Tube 6mm - Double - Silicone; Product Code: NZ3306-2;

Adept Medical Ltd recalls Otological Ventilation Tube - T-Tube 9mm - Silicone; Product Code: NZ3309;

FOREST RIVER CEDAR CREEK (2025) recall — Suspension