Product Recalls in Tennessee

Product recalls affecting Tennessee — including food, drugs, consumer products, medical devices, and vehicles distributed to Tennessee. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,115 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,115 in last 12 months

Showing 33613380 of 52,000 recalls

Medical DeviceJanuary 15, 2025· TERRAGENE S.A.

Recalled Item: ASP BIOTRACE Auto Read 60 Steam BI Process Challenge Device Recalled by...

The Issue: Error in the IFU lists an incorrect incubation time on one occasion of 20...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2025· Hologic, Inc

Recalled Item: Brand Name: Sertera Biopsy Device Product Name: Sertera Biopsy Device...

The Issue: Devices presented a condition in which the inner needle separated from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Single Use Guide Sheath Kits with the following product Recalled by...

The Issue: Potential for the radiopaque tip of the guide sheath component to...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 14, 2025· Draeger Medical Systems, Inc.

Recalled Item: Infinity Central Station. Model Number: MS26800 The Infinity CentralStation...

The Issue: Edifier speakers (shipped in or after April 2023) may not annunciate when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: AlluraXper FD20 System Code: (1) 722006 (2) 722012 (3) 722028 Recalled by...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: AlluraXperFD20/10 System Code: (1) 722029 Recalled by PHILIPS MEDICAL...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: AlluraXper FD20 Biplane System Code: (1) 722008 (2) 722013 Recalled by...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: AlluraXperFD20/15 System Code: (1) 722058 Recalled by PHILIPS MEDICAL...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 7 M20 System code: (1) 722224 (2) 722079 (3) Recalled by PHILIPS...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: AlluraXper FD20 OR Table System Code: (1) 722023 (2) 722035 Recalled by...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20 Biplane Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 3 M15 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura CV20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 7 M20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 3 M12 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20 Biplane OR Table Recalled by PHILIPS MEDICAL SYSTEMS...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20/15 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 5 M12 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20 OR Table Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing