Product Recalls in Iowa

Product recalls affecting Iowa — including food, drugs, consumer products, medical devices, and vehicles distributed to Iowa. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,475 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,475 in last 12 months

Showing 2236122380 of 49,990 recalls

FoodMay 20, 2019· Suja Life LLC

Recalled Item: Suja Organic Kombucha - Mixed Berries: 15.2 oz. glass bottle Recalled by...

The Issue: Firm has received complaints of finding pieces of glass in the products.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 20, 2019· Suja Life LLC

Recalled Item: Suja Organic Kombucha - Ginger Lemon: 15.2 oz. glass bottle Recalled by Suja...

The Issue: Firm has received complaints of finding pieces of glass in the products.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 20, 2019· Suja Life LLC

Recalled Item: Suja Organic Kombucha - Peach Ginger: 15.2 oz. glass bottle Recalled by Suja...

The Issue: Firm has received complaints of finding pieces of glass in the products.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 20, 2019· Teligent Pharma, Inc.

Recalled Item: Betamethasone Dipropionate Ointment USP Recalled by Teligent Pharma, Inc....

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 60 ARTICULATING EXTRA THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: SIGNIA TRI-STAPLE 2.0 BLACK 60MM EXTRA THICK RELOA Recalled by Covidien LLC...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· GE Healthcare, LLC

Recalled Item: Centricity PACS-IW with Universal Viewer version 5.0 Recalled by GE...

The Issue: There is a potential that one or more images or image series may be missing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· GE Healthcare, LLC

Recalled Item: Centricity Universal Viewer with PACS-IW foundation 6.0 Recalled by GE...

The Issue: There is a potential that one or more images or image series may be missing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 45 ARTICULATING XTRA THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Arrow International Inc

Recalled Item: Pediatric Two-Lumen Central Venous Catheterization Kit with Blue FlexTip...

The Issue: Lidstock contains a labeling error. The lidstock shows the catheter cross...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: SIGNIA TRI-STAPLE 2.0 CURVED TIP 45MM MEDIUM/ THIC Recalled by Covidien LLC...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: SIGNIA TRI-STAPLE 2.0 30MM MEDIUM/ THICK RELOAD Recalled by Covidien LLC Due...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 45 ARTICULATING MED THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA45 CT AR MD THK REL Recalled by Covidien LLC Due to The device may be...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 60 ARTICULATING MED THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 30 ARTICULATING MED THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: SIGNIA TRI-STAPLE 2.0 BLACK 45MM EXTRA THICK RELOA Recalled by Covidien LLC...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: SIGNIA TRI-STAPLE 2.0 CURVED TIP 60MM MEDIUM/ THIC Recalled by Covidien LLC...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 60 CURVED TIP ART MED THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
FoodMay 17, 2019· U.S. Tov, Inc.

Recalled Item: Global Pride Rattan Shoots in Brine: 24 oz. glass jar Recalled by U.S. Tov,...

The Issue: New York State Department of Agriculture and Markets sampled and tested...

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

Class I — Serious Health HazardOngoing
Refund