Product Recalls in Washington

Product recalls affecting Washington — including food, drugs, consumer products, medical devices, and vehicles distributed to Washington. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,824 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,824 in last 12 months

Showing 36813700 of 29,208 recalls

Medical DeviceJune 20, 2024· Securitas Healthcare LLC

Recalled Item: Arial Call Station Recalled by Securitas Healthcare LLC Due to There is a...

The Issue: There is a risk that alarms will not be received by the Arial Wireless...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2024· Securitas Healthcare LLC

Recalled Item: Arial Call Station Recalled by Securitas Healthcare LLC Due to This is a...

The Issue: This is a risk that alarms will not be received by the Arial Wireless Nurse...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2024· Luminex Corporation

Recalled Item: Verigene Gram Positive Blood Culture (BC-GP) Nucleic Acid Test Recalled by...

The Issue: Potential for defective test cartridges which may result in false positive...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2024· Cepheid

Recalled Item: Cepheid Recalled by Cepheid Due to Specimen collection device may leak after...

The Issue: Specimen collection device may leak after the patient sample swabs have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2024· Howmedica Osteonics Corp.

Recalled Item: UNITRAX Endoprosthesis Head Component - 42mm. Implantable component used in...

The Issue: Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2024· BioFire Diagnostics, LLC

Recalled Item: BIOFIRE Blood Culture Identification 2 (BCID2) Panel Recalled by BioFire...

The Issue: If blood culture identification panel is used in conjunction with specific...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2024· Howmedica Osteonics Corp.

Recalled Item: UNITRAX Endoprosthesis Head Component - 38mm. Implantable component used in...

The Issue: Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2024· Howmedica Osteonics Corp.

Recalled Item: UNITRAX Endoprosthesis Head Component - 43mm. Implantable component used in...

The Issue: Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2024· Foundation Medicine, Inc.

Recalled Item: FoundationOne Companion Diagnostic (F1CDx) Recalled by Foundation Medicine,...

The Issue: Two (2) reports were sent to customers with an incorrect negative claim on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2024· Angiodynamics, Inc.

Recalled Item: SOFT-VU KUMPE 5F X 65CM -Used for patients in need Recalled by...

The Issue: Mislabeled. The shelf-box labeling (unit of sale) is accurate for the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2024· Embecta Corp.

Recalled Item: BD Nano 2nd Gen Pen Needles 32G X 4mm (5-count Recalled by Embecta Corp. Due...

The Issue: BD Nano 2nd Gen Pen Needle was shipped close to or after the labeled...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2024· Angiodynamics, Inc.

Recalled Item: SOFT-VU KUMPE 5F X 40CM -Used for patients in need Recalled by...

The Issue: Mislabeled. The shelf-box labeling (unit of sale) is accurate for the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: Infusomat UNIV. 15 DROP PUMP SET W/ 3 ULTRASITE LL-Used Recalled by B. Braun...

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: OUTLOOK IV SET 15DROP W/2 CARESITE-Used with an electrically-powered...

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: Infusomat SPACE PUMP SET 15 DROP W/2 SAFEDAY-Used with an Recalled by B....

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: OUTLOOK PUMP SET 3 CARESITE LADS 133 IN.-Used with an Recalled by B. Braun...

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: Infusomat UNIV. 15 DROP PUMP SET Recalled by B. Braun Medical, Inc. Due to...

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: Infusomat 60DROP METRISET PUMP SET Recalled by B. Braun Medical, Inc. Due to...

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: Infusomat UNIV. 60 DROP PUMP SET Recalled by B. Braun Medical, Inc. Due to...

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: Infusomat UNIV. 15 DR PUMP SET Recalled by B. Braun Medical, Inc. Due to...

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing