Product Recalls in Idaho

Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 911 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
911 in last 12 months

Showing 47001–47020 of 48,215 recalls

Medical DeviceJuly 2, 2012· Ethicon, Inc.

Recalled Item: EVICEL Fibrin Sealant (Human) Rx Only. Manufacturer: Omrix...

The Issue: Ethicon and Omrix Biopharmaceuticals have received reports of air or gas...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2012· Greiner Bio-One North America, Inc.

Recalled Item: 3mL 9NC Coagulation Sodium Citrate 3.2% Recalled by Greiner Bio-One North...

The Issue: Part of the lot received a lower concentration of citrate solution which may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2012· Draeger Medical Systems, Inc.

Recalled Item: Drager PT 4000 Phototherapy System Recalled by Draeger Medical Systems, Inc....

The Issue: A routine internal quality check found that the Drager PT 4000 Phototherapy...

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

Class II — Potential Health HazardOngoing
DrugJuly 2, 2012· Hospira Inc.

Recalled Item: Carboplatin Injection Recalled by Hospira Inc. Due to Failed PH...

The Issue: Failed PH specification: The lots of Carboplatin Injection were manufactured...

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

Class III — Low RiskOngoing
Refund
DrugJuly 2, 2012· ASTRA ZENECA Lp

Recalled Item: Nexium (esomeprazole magnesium) Delayed-Release Capsules Recalled by ASTRA...

The Issue: Adulterated Presence of Foreign Tablets/Capsules: Some bottles may contain a...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 2, 2012· Merge Healthcare, Inc.

Recalled Item: Merge HEMO software. Recalled by Merge Healthcare, Inc. Due to The...

The Issue: The International Normalized Ratio (INR) value displayed in the study report...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2012· C.R. Bard, Inc., Urological Division

Recalled Item: Bard Foley procedural trays packaged in breather bags. The product Recalled...

The Issue: Incomplete seal on sterile packages of product.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2012· Arjo, Inc. dba ArjoHuntleigh

Recalled Item: Chorus Mobile Patient Lifter Recalled by Arjo, Inc. dba ArjoHuntleigh Due to...

The Issue: ArjoHuntleigh has received a limited number of customer reports concerning...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2012· CareFusion 303, Inc.

Recalled Item: Alaris Pump Module model 8100. Subsequent product code: FPA The Recalled by...

The Issue: The recall was initiated because Carefusion identified a potential risk...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 29, 2012· Arjo, Inc. dba ArjoHuntleigh

Recalled Item: Encore Mobile Patient Lifter Recalled by Arjo, Inc. dba ArjoHuntleigh Due to...

The Issue: ArjoHuntleigh has received a limited number of customer reports concerning...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2012· Arjo, Inc. dba ArjoHuntleigh

Recalled Item: Sara Plus Mobile Patient Lifter Recalled by Arjo, Inc. dba ArjoHuntleigh Due...

The Issue: ArjoHuntleigh has received a limited number of customer reports concerning...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2012· BD Biosciences, Systems & Reagents

Recalled Item: BD FACS 7-color Setup beads BD Biosciences Recalled by BD Biosciences,...

The Issue: Incorrect version of the CD was included with BD FACS 7 Color Setup Beads.

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

Class II — Potential Health HazardOngoing
FoodJune 29, 2012· Designer Protein LLC

Recalled Item: Designer Whey Chocolate Recalled by Designer Protein LLC Due to The recall...

The Issue: The recall was initiated because Designer Protein has confirmed that...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 29, 2012· Designer Protein LLC

Recalled Item: Designer Whey Strawberry Recalled by Designer Protein LLC Due to The recall...

The Issue: The recall was initiated because Designer Protein has confirmed that...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 29, 2012· Designer Protein LLC

Recalled Item: Designer Whey French Vanilla Recalled by Designer Protein LLC Due to The...

The Issue: The recall was initiated because Designer Protein has confirmed that...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 29, 2012· Lovin Oven, LLC

Recalled Item: Earth's Best Organic Wheat Teething Biscuits Recalled by Lovin Oven, LLC Due...

The Issue: Earth's Best is recalling Earth's Best Organic Wheat Teething Biscuits...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 29, 2012· Prometheus Laboratories Inc.

Recalled Item: Mercaptopurine Tablets Recalled by Prometheus Laboratories Inc. Due to...

The Issue: Failed USP Dissolution Test Requirements: The recalled lots do not meet the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 28, 2012· Health Plus Incorporated

Recalled Item: Super Colon Cleanse Recalled by Health Plus Incorporated Due to Labeling:...

The Issue: Labeling: Label Mix-up: The product is being recalled because active...

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

Class III — Low RiskOngoing
Refund
DrugJune 28, 2012· Mylan Pharmaceuticals Inc.

Recalled Item: Famotidine Tablets USP Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: Impurities/Degradation Products: Out of specification results for Related...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 28, 2012· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products DGXN Slides --- [REF] 834 3386. Product Recalled...

The Issue: Ortho Clinical Diagnostics revised the VITROS Chemistry Products DGXN Slides...

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

Class II — Potential Health HazardOngoing