Product Recalls in Indiana

Product recalls affecting Indiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Indiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,768 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,768 in last 12 months

Showing 23012320 of 29,228 recalls

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
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 7 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 FD20/10 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: Allura Xper FD10 - Catalog numbers: (1) 722003 Recalled by PHILIPS MEDICAL...

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 FD10C 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: Cardio Vascular-Allura Centron Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...

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 FD20/20 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 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: Allura Xper FD10/10 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: Allura CV20 System Code: 722031 Recalled by PHILIPS MEDICAL SYSTEMS...

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 3 M12 System Code: (1) 722063 (2) 722221 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 B12 System Code: (1) 722067 (2) 722225 (3) 722235 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: Azurion 7 B20 System Code: (1) 722068 (2) 722226 (3) 722236 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: 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: 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: 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