Product Recalls in Minnesota

Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,621 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,621 in last 12 months

Showing 1288112900 of 13,424 recalls

DrugFebruary 4, 2013· American Health Packaging

Recalled Item: buPROPion Hydrochloride Extended Release Tablets Recalled by American Health...

The Issue: Failed Stability Specifications; out of specification results at the 9 month...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 4, 2013· Carib Import & Export, Inc.

Recalled Item: Benjamins Infants Gripe Mixture Recalled by Carib Import & Export, Inc. Due...

The Issue: CGMP Deviations: this product is being recalled because an FDA inspection...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 1, 2013· Ferring Pharmaceuticals Inc

Recalled Item: TEV-TROPIN (somatropin (rDNA origin) for injection) 5 mg (15 IU). Recalled...

The Issue: Labeling: Label Mix-up: Units of Lot 201131320087 are packaged in cartons...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 1, 2013· Fresenius Kabi USA LLC (FK USA)

Recalled Item: CALCIUM GLUCONATE INJECTION Recalled by Fresenius Kabi USA LLC (FK USA) Due...

The Issue: Labeling: Missing label

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2013· Gilead Sciences, Inc.

Recalled Item: Vistide (cidofovir) Injection Recalled by Gilead Sciences, Inc. Due to...

The Issue: Presence of Particulate Matter: Particulate matter was found in some vials...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 31, 2013· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 31, 2013· Lupin Pharmaceuticals Inc.

Recalled Item: Suprax (cefixime for oral suspension) USP Recalled by Lupin Pharmaceuticals...

The Issue: Discoloration; Product may not meet specifications for color description...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 30, 2013· Mylan Pharmaceuticals Inc.

Recalled Item: Lansoprazole Delayed-release Capsules Recalled by Mylan Pharmaceuticals Inc....

The Issue: Presence of Foreign Tablets/Capsules: Bottles of lansoprazole 30 mg...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 25, 2013· Hospira Inc.

Recalled Item: Lactated Ringer's and 5% Dextrose Injection Recalled by Hospira Inc. Due to...

The Issue: Non-Sterility: Confirmed customer complaint of product contaminated with mold.

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 23, 2013· Mission Pharmacal Co

Recalled Item: Sodium Sulfacetamide 10% and Sulfur 5% Lotion Recalled by Mission Pharmacal...

The Issue: Superpotent: Drug product active ingredients were formulated incorrectly...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 23, 2013· Procter & Gamble Hair Care Llc

Recalled Item: Crest PRO-HEALTH CPC Antigingivitis/Antiplaque Oral Rinse Recalled by...

The Issue: Cross Contamination with Other Products: Product was mixed with another type...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 23, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Terazosin Hydrochloride Capsules Recalled by Teva Pharmaceuticals USA, Inc....

The Issue: Presence of Foreign Tablets/Capsules: Recall is being conducted due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 22, 2013· RX South LLC DBA RX3 Pharmacy

Recalled Item: Medi-bolic Booster Injectable (methionine 8.3 mg/mL Recalled by RX South LLC...

The Issue: CGMP Deviations: Pharmaceutical for injection was not manufactured according...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 22, 2013· Sandoz Incorporated

Recalled Item: Syeda (drospirenone and ethinyl estradiol) Recalled by Sandoz Incorporated...

The Issue: Tablet/Capsule Imprinted with Wrong ID; a portion of the tablets could...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 22, 2013· Fresenius Kabi USA LLC (FK USA)

Recalled Item: IRINOTECAN HYDROCHLORIDE INJECTION Recalled by Fresenius Kabi USA LLC (FK...

The Issue: Crystallization: Active pharmaceutical ingredient is precipitating in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2013· Aaron Industries Inc

Recalled Item: Rite Aid Maximum Strength Tussin Cough & Cold Mucus Relief CF Recalled by...

The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 18, 2013· Aaron Industries Inc

Recalled Item: Well at Walgreens Wal-Tussin CF Max Recalled by Aaron Industries Inc Due to...

The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 18, 2013· Aaron Industries Inc

Recalled Item: Wal-Mart Equate Tussin CF Adult Maximum Strength Recalled by Aaron...

The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 18, 2013· Aaron Industries Inc

Recalled Item: Select Brand Cough Control CF Max Recalled by Aaron Industries Inc Due to...

The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 17, 2013· Humco Holding Group, Inc

Recalled Item: Mercuroclear Antiseptic Anesthetic First Aid Helps prevent infection and...

The Issue: Microbial Contamination of Non-Sterile Product(s): The product has the...

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

Class II — Potential Health HazardOngoing
Refund