Product Recalls in Alabama

Product recalls affecting Alabama — including food, drugs, consumer products, medical devices, and vehicles distributed to Alabama. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,012 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
1,012 in last 12 months

Showing 26601–26620 of 50,591 recalls

Medical DeviceApril 9, 2018· Covidien LLC

Recalled Item: EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 4.8MM...

The Issue: There is a potential for improper welding of the yellow staple guide to the...

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

Class II — Potential Health HazardOngoing
DrugApril 6, 2018· Sandoz Incorporated

Recalled Item: Triamterene and Hydrochlorothiazide Tablets Recalled by Sandoz Incorporated...

The Issue: Cross Contamination With Other Products: presence of unrelated ingredients...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodApril 6, 2018· The J.M. Smucker Company, Inc.

Recalled Item: HUNGRY JACK Original PANCAKE & WAFFLE MIX NET WT 32 OZ (2 LB) 907 g Recalled...

The Issue: Product tested positive for salmonella.

Recommended Action: Do not consume. Return to store for a refund or discard.

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

Recalled Item: OviTex 1S Reinforced BioScaffold 4x8cm 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 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