Product Recalls in Florida

Product recalls affecting Florida — including food, drugs, consumer products, medical devices, and vehicles distributed to Florida. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,801 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,801 in last 12 months

Showing 1728117300 of 30,686 recalls

Medical DeviceApril 6, 2018· AROA Biosurgery, LTD.

Recalled Item: OviTex Reinforced BioScaffold 6x10cm 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 2S Reinforced BioScaffold 10x12cm 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 10x12cm 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 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· AROA Biosurgery, LTD.

Recalled Item: OviTex Reinforced BioScaffold 10x20cm 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 2S Reinforced BioScaffold 10x12cm 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 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 2S 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 1S 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 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