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. 2,660 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,660 in last 12 months

Showing 27012720 of 49,990 recalls

Medical DeviceMarch 24, 2025· Zimmer, Inc.

Recalled Item: Zimmer Biomet Ceramic Head Recalled by Zimmer, Inc. Due to The associated...

The Issue: The associated product labeling does not adequately provide compatibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Zimmer, Inc.

Recalled Item: Zimmer Biomet Ceramic Head Recalled by Zimmer, Inc. Due to The associated...

The Issue: The associated product labeling does not adequately provide compatibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Zimmer, Inc.

Recalled Item: Zimmer Biomet Ceramic Head Recalled by Zimmer, Inc. Due to The associated...

The Issue: The associated product labeling does not adequately provide compatibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Zimmer, Inc.

Recalled Item: Zimmer Biomet Ceramic Head Recalled by Zimmer, Inc. Due to The associated...

The Issue: The associated product labeling does not adequately provide compatibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Zimmer, Inc.

Recalled Item: Zimmer Biomet Ceramic Head Recalled by Zimmer, Inc. Due to The associated...

The Issue: The associated product labeling does not adequately provide compatibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Baxter Healthcare Corporation

Recalled Item: Welch Allyn Connex Vital Signs Monitor (CVSM): Recalled by Baxter Healthcare...

The Issue: There were customer reports of devices which experienced battery-related...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Baxter Healthcare Corporation

Recalled Item: Welch Allyn CONNEX Accessory Power Management Stand: Recalled by Baxter...

The Issue: There were customer reports of devices which experienced battery-related...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Baxter Healthcare Corporation

Recalled Item: Welch Allyn CP150 Electrocardiograph: Recalled by Baxter Healthcare...

The Issue: There were customer reports of devices which experienced battery-related...

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

Class II — Potential Health HazardOngoing
DrugMarch 21, 2025· Somerset Therapeutics Private Limited

Recalled Item: Haloperidol Decanoate Injection 100mg/mL Recalled by Somerset Therapeutics...

The Issue: Lack of Assurance of Sterility: Media fill with bacterial contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 21, 2025· Somerset Therapeutics Private Limited

Recalled Item: Haloperidol Decanoate Injection 50mg/mL Recalled by Somerset Therapeutics...

The Issue: Lack of Assurance of Sterility: Media fill with bacterial contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 21, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Venlafaxine Tablets Recalled by Zydus Pharmaceuticals (USA) Inc Due to...

The Issue: Presence of Foreign Substance: Product complaint received for the presence...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 21, 2025· Somerset Therapeutics Private Limited

Recalled Item: Methocarbamol Injection USP 1 Recalled by Somerset Therapeutics Private...

The Issue: Lack of Assurance of Sterility: Media fill with bacterial contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 21, 2025· Somerset Therapeutics Private Limited

Recalled Item: Haloperidol Decanoate Injection Recalled by Somerset Therapeutics Private...

The Issue: Lack of Assurance of Sterility: Media fill with bacterial contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 21, 2025· Somerset Therapeutics Private Limited

Recalled Item: Haloperidol Decanoate Injection 50mg/mL Recalled by Somerset Therapeutics...

The Issue: Lack of Assurance of Sterility: Media fill with bacterial contamination

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare CARESTATION 650C A1 Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare CARESTATION 620 A2 Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare CARESTATION 750 A2 Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare Carestation 650 SE Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare Carestation 620 A1 Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare CARESTATION 650 A2 Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing