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. 2,447 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,447 in last 12 months

Showing 2734127360 of 49,990 recalls

FoodDecember 18, 2017· Gel Spice Co, Inc.

Recalled Item: Spice Supreme Beef Flavored Bouillon Cubes 1.7 oz (48 g) Recalled by Gel...

The Issue: Gel Spice, Inc. is recalling three beef flavored bouillon cube products...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 18, 2017· Gel Spice Co, Inc.

Recalled Item: Spice Supreme Beef Flavored Bouillon Cubes 1.7 oz (48 g) Recalled by Gel...

The Issue: Gel Spice, Inc. is recalling three beef flavored bouillon cube products...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 18, 2017· Johnson & Johnson Vision Care, Inc.

Recalled Item: ACUVUE OASYS for ASTIGMATISM Brand Contact Lenses. Lot no. B00NKM0G....

The Issue: Package integrity failure observed during routine shift package integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur TSH3-Ultra (Thyroid Stimulating Hormone 3 Ultra) Recalled by...

The Issue: In certain scenarios the ADVIA Centaur CP, XP and XPT immunoassay analyzers...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur BNP (B-type Natriuretic Peptide) Recalled by Siemens...

The Issue: In certain scenarios the ADVIA Centaur CP, XP and XPT immunoassay analyzers...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2017· Phadia US Inc

Recalled Item: ImmunoCAP Allergen c5 Recalled by Phadia US Inc Due to The stability...

The Issue: The stability specifications of ImmunoCAP Allergen c5, Ampicilloyl were not met.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2017· Phadia US Inc

Recalled Item: ImmunoCAP Allergen c6 Recalled by Phadia US Inc Due to The stability...

The Issue: The stability specifications of ImmunoCAP Allergen c6, Amoxicilloyl were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2017· Roche Diagnostics Corporation

Recalled Item: c6000 Recalled by Roche Diagnostics Corporation Due to Complaints have been...

The Issue: Complaints have been received concerning questionable results on analyzers...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2017· Roche Diagnostics Corporation

Recalled Item: cobas e 411 Immunoassay Analyzer (Discrete Photometric Analyzer for Clinical...

The Issue: Complaints have been received concerning questionable results on analyzers...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2017· Roche Diagnostics Corporation

Recalled Item: Modular E 170 Analyzer: Immunoassay Chemistry Analyzer Recalled by Roche...

The Issue: Complaints have been received concerning questionable results on analyzers...

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

Class II — Potential Health HazardOngoing
DrugDecember 15, 2017· Amneal Pharmaceuticals

Recalled Item: Fosphenytoin Sodium Injection Recalled by Amneal Pharmaceuticals Due to...

The Issue: Presence of particulate matter

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 15, 2017· Akorn Inc

Recalled Item: Gabapentin Oral Solution Recalled by Akorn Inc Due to CGMP Deviations:...

The Issue: CGMP Deviations: Inadvertent release of a drug product with unapproved...

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

Class III — Low RiskOngoing
Refund
DrugDecember 15, 2017· B. Braun Medical Inc

Recalled Item: 0.25% Acetic Acid Irrigation USP Recalled by B. Braun Medical Inc Due to...

The Issue: Presence of Particulate Matter: identified as polyethylene, which is...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 15, 2017· GE Healthcare, LLC

Recalled Item: Uterine Electromyographic Monitor -Monica IF24 Interface System Product...

The Issue: if the cables of the Monica IF24 System are removed by a user, and then...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2017· GE Healthcare, LLC

Recalled Item: Uterine Electromyographic Monitor - Monica Novii Wireless Patch System...

The Issue: if the cables of the Monica Novii System are removed by a user, and then...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView Model 882480 Product Usage: BrightView and BrightView X are...

The Issue: During collimator exchange, the alignment of the collimator cart and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Precedence 6 Model # 882351 Product Usage: Precedence (cleared as Recalled...

The Issue: During collimator exchange, the alignment of the collimator cart and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView XCT Model 882482 Product Usage: BrightView XCT is a Recalled by...

The Issue: During collimator exchange, the alignment of the collimator cart and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView X Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: During collimator exchange, the alignment of the collimator cart and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Precedence 16 Model # 882350 Product Usage: Precedence (cleared as Recalled...

The Issue: During collimator exchange, the alignment of the collimator cart and...

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

Class II — Potential Health HazardOngoing