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. 1,757 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
1,757 in last 12 months

Showing 4128141300 of 48,215 recalls

DrugApril 18, 2014· Hospira Inc.

Recalled Item: 1% LIDOCAINE HCl Injection Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Confirmed customer complaint that orange and...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 18, 2014· Med-Mizer, Inc.

Recalled Item: RetractaBed Recalled by Med-Mizer, Inc. Due to All configurations of the SS...

The Issue: All configurations of the SS Retractabed, Clinical Contour, made prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2014· Med-Mizer, Inc.

Recalled Item: RetractaBed Recalled by Med-Mizer, Inc. Due to All configurations of the SS...

The Issue: All configurations of the SS Retractabed, Clinical Contour, made prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2014· Med-Mizer, Inc.

Recalled Item: RetractaBed Recalled by Med-Mizer, Inc. Due to All configurations of the SS...

The Issue: All configurations of the SS Retractabed, Clinical Contour, made prior to...

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

Class II — Potential Health HazardOngoing
FoodApril 18, 2014· Woeber Mustard Manufacturing Co Inc

Recalled Item: Hickory Farms Chipotle Ranch Sauce Recalled by Woeber Mustard Manufacturing...

The Issue: Unlabeled milk allergen.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 17, 2014· Mckesson Medical Immaging

Recalled Item: McKesson Radiology-PACS. McKesson Radiology is a medical image and...

The Issue: High priority alert icon was not displayed in the Study List when there are...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2014· Gen-Probe Inc

Recalled Item: APTIMA Urine Collection Kit Recalled by Gen-Probe Inc Due to Incorrect...

The Issue: Incorrect labeling was used on each pouch of the affected lots of APTIMA...

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

Class III — Low RiskOngoing
DrugApril 17, 2014· Trigen Laboratories, Inc.

Recalled Item: Triveen - PRx RNF Capsules Recalled by Trigen Laboratories, Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Label indicates that the product...

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

Class III — Low RiskOngoing
Refund
DrugApril 17, 2014· Cubist Pharmaceuticals, Inc.

Recalled Item: CUBICIN (daptomycin for injection) Recalled by Cubist Pharmaceuticals, Inc....

The Issue: Presence of Particulate Matter: Customer complaint stating that one vial...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 17, 2014· Wockhardt Usa Inc.

Recalled Item: Wockhardt Metoprolol Succinate Recalled by Wockhardt Usa Inc. Due to Failed...

The Issue: Failed Dissolution Specifications: Product was out of specification (OOS) at...

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

Class III — Low RiskOngoing
Refund
DrugApril 16, 2014· Pfizer Us Pharmaceutical Group

Recalled Item: Pristiq (desvenlafaxine) Extended-Release Tablets 50 mg Recalled by Pfizer...

The Issue: Presence of Foreign Tablets/Capsules: Pfizer is recalling 50 mg Pristiq...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 16, 2014· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 PT/INR Professional Test Strips Recalled by Alere San Diego,...

The Issue: Test Strips may report an inaccurately low INR result. Several patients had...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 16, 2014· Maquet Medical Systems USA

Recalled Item: Maquet PowerLED 700. Product Usage Recalled by Maquet Medical Systems USA...

The Issue: Maquet has identified an issue with the Maquet PowerLED 700 (certain serial...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2014· Synthes, Inc.

Recalled Item: DePuy Synthes Craniomaxillofacial Distraction System (AB Distractor Bodies...

The Issue: DePuy Synthes is initiating a recall of certain lots of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 16, 2014· Sakura Finetek USA Inc

Recalled Item: Tissue-Tek PARAFORM PROC/EMB/MEDIUM Recalled by Sakura Finetek USA Inc Due...

The Issue: This Lot has variations in melting temperature.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2014· Biomet, Inc.

Recalled Item: EZPass Nylon Monofilament Single Pack Recalled by Biomet, Inc. Due to The...

The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2014· Biomet, Inc.

Recalled Item: EZPass Suture Retriever Recalled by Biomet, Inc. Due to The nitinol wire or...

The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2014· Brainlab AG

Recalled Item: ExacTrac 5.5 Recalled by Brainlab AG Due to When using a specific plan...

The Issue: When using a specific plan update workflow in combination with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2014· Fisher & Paykel Healthcare, Ltd.

Recalled Item: Infant Nasal CPAP (continuous positive airway pressure) Prong Recalled by...

The Issue: The Infant Nasal CPAP Prong has the potential to detach from the Nasal...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 15, 2014· Biomet, Inc.

Recalled Item: EZPass Passer Recalled by Biomet, Inc. Due to The nitinol wire or...

The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...

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

Class II — Potential Health HazardOngoing