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. 1,693 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
1,693 in last 12 months

Showing 4242142440 of 48,215 recalls

FoodNovember 8, 2013· Plum Inc

Recalled Item: Plum Organics Tots Blueberry Oats & Quinoa Morning Mish Mash Recalled by...

The Issue: Manufacturing defect leading to post-process contamination.

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 8, 2013· Plum Inc

Recalled Item: Plum Recalled by Plum Inc Due to Manufacturing defect leading to...

The Issue: Manufacturing defect leading to post-process contamination.

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 8, 2013· Plum Inc

Recalled Item: Plum Organics Spinach Recalled by Plum Inc Due to Manufacturing defect...

The Issue: Manufacturing defect leading to post-process contamination.

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 8, 2013· Vega / Sequel Naturals

Recalled Item: Vega Sport Performance Protein Dietary Supplement Vanilla Powder....

The Issue: Sequel Naturals is recalling nine lots of products due to contamination by...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 8, 2013· Plum Inc

Recalled Item: Plum Organics Green Bean Recalled by Plum Inc Due to Manufacturing defect...

The Issue: Manufacturing defect leading to post-process contamination.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 8, 2013· Fresenius Kabi USA, LLC

Recalled Item: PACLITAXEL INJECTION Recalled by Fresenius Kabi USA, LLC Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Package Insert- Missing text on the product...

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

Class III — Low RiskOngoing
Refund
DrugNovember 8, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Valacyclovir Hydrochloride Tablets Recalled by Teva Pharmaceuticals USA,...

The Issue: Presence of Foreign Tablets/Capsules: Potential of Pravastatin tablet...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 7, 2013· West-Ward Pharmaceutical Corp.

Recalled Item: Carisoprodol Tablets Recalled by West-Ward Pharmaceutical Corp. Due to...

The Issue: Presence of Foreign Substance; heavy metals (chromium, titanium etc) and...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 7, 2013· Deseo Rebajar

Recalled Item: Adipotrim XT Recalled by Deseo Rebajar Due to Undeclared Api

The Issue: Marketed Without an Approved NDA/ANDA: FDA lab results found undeclared API...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 7, 2013· EOS Imaging

Recalled Item: EOS System X- ray beam Digital radiography system used in Recalled by EOS...

The Issue: EOS imaging discovered during production internal testing that the X-ray...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2013· GE Healthcare, LLC

Recalled Item: GE Optima XR220amx and Optima XR200amx with Digital Upgrade Mobile Recalled...

The Issue: There exists a software issue associated with patient selection from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2013· OrthoPediatrics Corp

Recalled Item: OrthoPediatrics ACL Reconstruction System is a pediatric and small stature...

The Issue: Part # 01-1008-0040/0047, ACL Sleeve Installation/ Insertion Tool, shipped...

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

Class II — Potential Health HazardOngoing
FoodNovember 7, 2013· NOW Foods

Recalled Item: Digestive enzyme capsules sold under the NOW Foods Recalled by NOW Foods Due...

The Issue: Digestive enzyme capsules manufactured by NOW Foods may contain the...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 7, 2013· Ortho Molecular Products Inc

Recalled Item: Ortho Molecular Products DigestzymeV. Dietary Supplement. Gastrointestinal...

The Issue: Ortho Molecular Products' vegetable enzyme vendor issued a recall of the raw...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2013· Actavis Elizabeth LLC

Recalled Item: Clonazepam Tablets Recalled by Actavis Elizabeth LLC Due to Subpotent Drug:...

The Issue: Subpotent Drug: During routine stability testing one tablet was found with...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2013· GlaxoSmithKline, LLC.

Recalled Item: Imitrex STATdose System Recalled by GlaxoSmithKline, LLC. Due to Lack of...

The Issue: Lack of Assurance of Sterility: A small number of pre-filled syringes may...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2013· Sandoz Inc

Recalled Item: Bumetanide Tablets USP 0.5 mg. Rx Only Recalled by Sandoz Inc Due to Failed...

The Issue: Failed Moisture Limit; Out of Specification (OOS) results were obtained for...

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

Class III — Low RiskOngoing
Refund
DrugNovember 6, 2013· GlaxoSmithKline, LLC.

Recalled Item: Sumatriptan Succinate Injection Recalled by GlaxoSmithKline, LLC. Due to...

The Issue: Lack of Assurance of Sterility: A small number of pre-filled syringes may...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 6, 2013· Data Innovations, Inc.

Recalled Item: Instrument Manager driver : Driver sysu100i that connects to the Recalled by...

The Issue: When connected to the Sysmex UF-100, the Instrument Manager driver sysu100i...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2013· Karl Storz Endoscopy America Inc

Recalled Item: Axillent Debakey Grasping Forceps Recalled by Karl Storz Endoscopy America...

The Issue: KARL STORZ is recalling the Axillent Debakey Grasping Forceps because the...

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

Class II — Potential Health HazardOngoing