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. 2,547 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,547 in last 12 months

Showing 2760127620 of 53,528 recalls

Medical DeviceApril 6, 2018· AROA Biosurgery, LTD.

Recalled Item: OviTex Reinforced BioScaffold 4x8cm Recalled by AROA Biosurgery, LTD. Due to...

The Issue: Degradation of the PGA suture material used in the manufacture of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· AROA Biosurgery, LTD.

Recalled Item: OviTex 2S Reinforced BioScaffold 6x10cm Recalled by AROA Biosurgery, LTD....

The Issue: Degradation of the PGA suture material used in the manufacture of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· AROA Biosurgery, LTD.

Recalled Item: OviTex 2S Reinforced BioScaffold 20x20cm Recalled by AROA Biosurgery, LTD....

The Issue: Degradation of the PGA suture material used in the manufacture of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· AROA Biosurgery, LTD.

Recalled Item: OviTex 1S Reinforced BioScaffold 6x10cm Recalled by AROA Biosurgery, LTD....

The Issue: Degradation of the PGA suture material used in the manufacture of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· AROA Biosurgery, LTD.

Recalled Item: OviTex Reinforced BioScaffold 20x20cm Recalled by AROA Biosurgery, LTD. Due...

The Issue: Degradation of the PGA suture material used in the manufacture of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· AROA Biosurgery, LTD.

Recalled Item: OviTex Reinforced BioScaffold 16x20cm Recalled by AROA Biosurgery, LTD. Due...

The Issue: Degradation of the PGA suture material used in the manufacture of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· AROA Biosurgery, LTD.

Recalled Item: OviTex Reinforced BioScaffold 18x22cm Recalled by AROA Biosurgery, LTD. Due...

The Issue: Degradation of the PGA suture material used in the manufacture of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· AROA Biosurgery, LTD.

Recalled Item: OviTex 1S Reinforced BioScaffold 16x20cm Recalled by AROA Biosurgery, LTD....

The Issue: Degradation of the PGA suture material used in the manufacture of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· AROA Biosurgery, LTD.

Recalled Item: OviTex 1S Reinforced BioScaffold 10x20cm Recalled by AROA Biosurgery, LTD....

The Issue: Degradation of the PGA suture material used in the manufacture of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· AROA Biosurgery, LTD.

Recalled Item: OviTex Reinforced BioScaffold 10x12cm Recalled by AROA Biosurgery, LTD. Due...

The Issue: Degradation of the PGA suture material used in the manufacture of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· AROA Biosurgery, LTD.

Recalled Item: OviTex 1S Reinforced BioScaffold 18x22cm Recalled by AROA Biosurgery, LTD....

The Issue: Degradation of the PGA suture material used in the manufacture of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: T-Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: Straight Plate Recalled by Orthofix, Inc Due to Firm is conducting a...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: TN Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: Box Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: Rival Reduce Kit Locking and Non-Locking Screw D 2.0MM Recalled by Orthofix,...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: Y-Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: L-Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: Rival View Kit Locking and Non-Locking Screw D 2.7MM Recalled by Orthofix,...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: Lapidus Plate Recalled by Orthofix, Inc Due to Firm is conducting a...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing