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. 1,069 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
1,069 in last 12 months

Showing 15881–15900 of 49,990 recalls

Medical DeviceApril 26, 2021· Alphatec Spine, Inc.

Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...

The Issue: There is a potential for the screw blocking mechanism on the anterior...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2021· Alphatec Spine, Inc.

Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...

The Issue: There is a potential for the screw blocking mechanism on the anterior...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2021· Alphatec Spine, Inc.

Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...

The Issue: There is a potential for the screw blocking mechanism on the anterior...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2021· Alphatec Spine, Inc.

Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...

The Issue: There is a potential for the screw blocking mechanism on the anterior...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2021· Alphatec Spine, Inc.

Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...

The Issue: There is a potential for the screw blocking mechanism on the anterior...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2021· Alphatec Spine, Inc.

Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...

The Issue: There is a potential for the screw blocking mechanism on the anterior...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2021· Alphatec Spine, Inc.

Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...

The Issue: There is a potential for the screw blocking mechanism on the anterior...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2021· Alphatec Spine, Inc.

Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...

The Issue: There is a potential for the screw blocking mechanism on the anterior...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2021· Alphatec Spine, Inc.

Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...

The Issue: There is a potential for the screw blocking mechanism on the anterior...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2021· Alphatec Spine, Inc.

Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...

The Issue: There is a potential for the screw blocking mechanism on the anterior...

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

Class II — Potential Health HazardOngoing
DrugApril 26, 2021· Teva Pharmaceuticals USA

Recalled Item: Methylprednisolone Acetate Injectable Suspension USP Recalled by Teva...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 26, 2021· Teva Pharmaceuticals USA

Recalled Item: Haloperidol Decanoate Injection Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 26, 2021· Teva Pharmaceuticals USA

Recalled Item: Leucovorin Calcium for Injection Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 26, 2021· Teva Pharmaceuticals USA

Recalled Item: Metoclopramide Injection USP Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 26, 2021· Teva Pharmaceuticals USA

Recalled Item: Haloperidol Decanoate Injection Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 22, 2021· GOLDEN MEDAL MUSHROOM INC

Recalled Item: Enoki Mushroom Product of Korea Net Wt. 200 g/7.05 oz. Recalled by GOLDEN...

The Issue: Michigan Department of Agriculture and Rural Development sampled product and...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 22, 2021· Remel Inc

Recalled Item: Remel Bile Esculin Azide Agar w/ 6mcg/ml Vancomycin Recalled by Remel Inc...

The Issue: The media allows growth of E. faecalis ATCC 29212 with blackening of the media.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2021· Welch Allyn Inc

Recalled Item: ProBP 3400 Digital Blood Pressure Device ((handheld Recalled by Welch Allyn...

The Issue: Potential Risk of fluid ingress to the power supplies, resulting in risk of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2021· Welch Allyn Inc

Recalled Item: GS777 Wall Transformer Model: 77710 Intended Use: The GS777 Wall Recalled by...

The Issue: Potential Risk of fluid ingress to the power supplies, resulting in risk of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2021· MICROVENTION INC.

Recalled Item: VIA Microcatheter VIA 27 - Product Usage: is Recalled by MICROVENTION INC....

The Issue: Due to inadvertently shipping to U.S. customers with international labeling...

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

Class III — Low RiskOngoing