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. 2,589 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,589 in last 12 months

Showing 1286112880 of 13,371 recalls

DrugDecember 22, 2012· D& S Herbals, LLC

Recalled Item: Super Power capsules Recalled by D& S Herbals, LLC Due to Marketed Without...

The Issue: Marketed Without An Approved NDA/ANDA: This dietary supplement has been...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 21, 2012· Lee Pharmaceuticals, Inc

Recalled Item: 12-Hour Sinus (oxymetazoline hydrochloride) Nasal Spray Recalled by Lee...

The Issue: Microbial Contamination of a Non-Sterile Products: 12-Hour Sinus Nasal Spray...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2012· Warner Chilcott Company LLC

Recalled Item: Femtrace 0.45 mg (Estradiol Acetate) Tablets Recalled by Warner Chilcott...

The Issue: Failed Impurity/Degradation Specifications due to moisture ingress in...

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

Class III — Low RiskOngoing
Refund
DrugDecember 21, 2012· Warner Chilcott Company LLC

Recalled Item: Femtrace 0.9 mg (Estradiol Acetate) Tablets Recalled by Warner Chilcott...

The Issue: Failed Impurity/Degradation Specifications due to moisture ingress in...

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

Class III — Low RiskOngoing
Refund
DrugDecember 18, 2012· Belmora LLC

Recalled Item: Flanax (aluminum hydroxide Recalled by Belmora LLC Due to Defective...

The Issue: Defective Container: Product lacks tamper evident breakaway band on cap.

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

Class III — Low RiskOngoing
Refund
DrugDecember 18, 2012· Matrixx Initiatives Inc

Recalled Item: Zicam Extreme Congestion Relief (oxymetazoline HCl) nasal gel Recalled by...

The Issue: Microbial Contamination of Non-Sterile Products: Product may be contaminated...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 18, 2012· Watson Pharmaceuticals

Recalled Item: Taztia XT(diltiazem HCI extended release capsules Recalled by Watson...

The Issue: Failed Dissolution Specification: Out of a specification result occurred...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: libigrow capsules Recalled by Performance Plus Marketing, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 17, 2012· Pacira Pharmaceuticals, Inc.

Recalled Item: EXPAREL (bupivacaine liposome injectable suspension) Recalled by Pacira...

The Issue: Subpotent; bupivacaine

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: BLUE Diamond Pill Recalled by Performance Plus Marketing, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: libigrow XXXTREME Capsules Recalled by Performance Plus Marketing, Inc. Due...

The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: BLUE Diamond PLATINUM Capsules Recalled by Performance Plus Marketing, Inc....

The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: Mojo nights Capsules Recalled by Performance Plus Marketing, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: CASANOVA Capsules Recalled by Performance Plus Marketing, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: Mojo nights SUPREME Capsules Recalled by Performance Plus Marketing, Inc....

The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 17, 2012· L. Perrigo Co.

Recalled Item: Prednisone tablets Recalled by L. Perrigo Co. Due to Presence of Foreign...

The Issue: Presence of Foreign Substance(s); Perrigo has been notified of a recall by...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2012· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Hydrocodone Bitartrate and Acetaminophen Tablets Recalled by Mylan...

The Issue: Superpotent (Multiple Ingredient) Drug: Oversized tablets resulting in...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 13, 2012· Watson Laboratories Inc

Recalled Item: Caziant (desogestrel and ethinyl estradiol) Tablets Recalled by Watson...

The Issue: Impurities/Degradation Products: Out-of-specification results were obtained...

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

Class III — Low RiskOngoing
Refund
DrugDecember 12, 2012· Schering-Plough Products, LLC

Recalled Item: Temodar (temozolomide) Capsule Recalled by Schering-Plough Products, LLC Due...

The Issue: Failed Impurities/Degradation Specifications: The recall is being initiated...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 12, 2012· Boehringer Ingelheim Roxane Inc

Recalled Item: Perindopril Erbumine Tablets Recalled by Boehringer Ingelheim Roxane Inc Due...

The Issue: Impurities/Degradation Products: Out of Specification results found for...

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

Class III — Low RiskOngoing
Refund