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. 2,459 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,459 in last 12 months

Showing 2450124520 of 49,990 recalls

DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: Tri-Mix Papaverine/Phentolamine/Alprostadil 150 mg/5 mg/50 mcg a) Injectable...

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
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: HCG 50 Recalled by Pharm D Solutions, LLC Due to Lack of Assurance of Sterility

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
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: Sermorelin/GHRP-2 18 mg/6 mg powder Recalled by Pharm D Solutions, LLC Due...

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
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: Sermorelin/GHRP-2/GHRP-6 Mannitol 9 mg/9 mg/9 mg/300 mg Powder Recalled by...

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
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: Phenol 5% and Glycerin Aqueous Solution 10 mL Injection Recalled by Pharm D...

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
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: Bi-Mix Injection Recalled by Pharm D Solutions, LLC Due to Lack of Assurance...

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
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: Trimix Papaverine/Phentolamine/Alprostadil 30 mg/1 mg/10 mcg Powder Pharm D...

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
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: Trimix T-101 Alprostadil/Phapaverine/Phentolamine 5.9 mcg/17.65...

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
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: Slenderella Compound Injectable Recalled by Pharm D Solutions, LLC 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
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: Calcium Gluconate 2.5% a) 250 mL 25 mg/mL NDC 69699-0908-25 Recalled by...

The Issue: Lack of Assurance of Sterility

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

Class III — Low RiskOngoing
Refund
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: Sermorelin/GHRP-2 9 mg/9 mg Powder Recalled by Pharm D Solutions, LLC 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
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: HCG Lyophilized 5000 IU Injectable Pharm D Solutions Recalled by Pharm D...

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
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: Glutamine 10 mg/mL Solution Recalled by Pharm D Solutions, LLC Due to Lack...

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
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: Trimix BM3 Papaverine 30 mg/Phentolamine 1 mg Injectable Recalled by Pharm D...

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
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: HCG 4000 Unit Injectable Recalled by Pharm D Solutions, LLC Due to Lack of...

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
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: Trimix T 101 Alprostadil/Papverine/Phentolamine 5.9 mcg/17.65 mg/0.59 mcg...

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
Medical DeviceSeptember 10, 2018· GE Healthcare Biosciences

Recalled Item: DeltaVision OMX SR Imaging System Model Number: 29115476 The DeltaVision...

The Issue: Non-conformance with the DeltaVision OMX SR, the interlocks are not wired in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2018· Boston Scientific Corporation

Recalled Item: VALITUDE X4 CRT-P (Cardiac Resynchronization Therapy Pacemaker) Recalled by...

The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2018· Boston Scientific Corporation

Recalled Item: PROPONENT Pacemaker Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2018· Boston Scientific Corporation

Recalled Item: ACCOLADE Pacemaker Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...

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

Class II — Potential Health HazardOngoing