Product Recalls in Indiana

Product recalls affecting Indiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Indiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,456 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,456 in last 12 months

Showing 4420144220 of 53,528 recalls

Medical DeviceJune 19, 2014· Abbott Molecular

Recalled Item: 5 mL Reaction Vessels (a consumable of the Abbott m2000sp Recalled by Abbott...

The Issue: Abbott Molecular identified that some of the 5 ml Reaction Vessels (RVs)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2014· Boston Scientific CRM Corp

Recalled Item: Boston Scientific ENDOTAK RELIANCE¿ SG Recalled by Boston Scientific CRM...

The Issue: A review of manufacturing test records for Boston Scientific ENDOTAK...

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

Class II — Potential Health HazardOngoing
FoodJune 18, 2014· Land O' Lakes, Inc

Recalled Item: Item: 48135 Land O'Lakes Recalled by Land O' Lakes, Inc Due to Land O'Lakes...

The Issue: Land O'Lakes is recalling certain cheese products due to potential...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 18, 2014· Land O' Lakes, Inc

Recalled Item: Item: 48770 Land O'Lakes Recalled by Land O' Lakes, Inc Due to Land O'Lakes...

The Issue: Land O'Lakes is recalling certain cheese products due to potential...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 18, 2014· Land O' Lakes, Inc

Recalled Item: Item: 48775 Land O'Lakes Recalled by Land O' Lakes, Inc Due to Land O'Lakes...

The Issue: Land O'Lakes is recalling certain cheese products due to potential...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 18, 2014· Land O' Lakes, Inc

Recalled Item: Item: 4815 Land O'Lakes Recalled by Land O' Lakes, Inc Due to Land O'Lakes...

The Issue: Land O'Lakes is recalling certain cheese products due to potential...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 17, 2014· Hospira Inc.

Recalled Item: Marcaine (bupivacaine HCl) injection Recalled by Hospira Inc. Due to...

The Issue: Presence of Particulate Matter: Confirmed customer complaint of discolored...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 17, 2014· Teva Pharmaceuticals USA

Recalled Item: Velivet (desogestrel and ethinyl estradiol tablets - triphasic regimen)...

The Issue: Failed Impurities/Degradation Specifications: out of specification impurity...

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

Class III — Low RiskOngoing
Refund
DrugJune 17, 2014· Teva Pharmaceuticals USA

Recalled Item: Apri (desogestrel and ethinyl estradiol tablets USP) Recalled by Teva...

The Issue: Failed Impurities/Degradation Specifications: out of specification impurity...

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

Class III — Low RiskOngoing
Refund
DrugJune 17, 2014· Teva Pharmaceuticals USA

Recalled Item: Kariva (desogestrel/ethinyl estradiol and ethinyl estradiol) Tablets 0.15...

The Issue: Failed Impurities/Degradation Specifications: out of specification impurity...

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

Class III — Low RiskOngoing
Refund
DrugJune 17, 2014· Teva Pharmaceuticals USA

Recalled Item: Mircette (desogestrel/ethinyl estradiol and ethinyl estradiol) Tablets 0.15...

The Issue: Failed Impurities/Degradation Specifications: out of specification impurity...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 17, 2014· Varian Medical Systems, Inc.

Recalled Item: C-Series High Energy Linear Accelerator - Models: Novalis Tx Recalled by...

The Issue: Trend in reports of unexpected decrease in beam output in C-series High...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2014· Baxter Healthcare Corp.

Recalled Item: Baxter MiniCap with Povidone-Iodine Solution Recalled by Baxter Healthcare...

The Issue: Inadequate iodine and packaging related defects.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo¿ Advanced Perfusion System 1 220/240V AC Recalled by Terumo...

The Issue: An evaluation of the APS1 Operator Manual found that existing instructions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo¿ Advanced Perfusion System 1 100/120V AC Recalled by Terumo...

The Issue: An evaluation of the APS1 Operator Manual found that existing instructions...

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

Class II — Potential Health HazardOngoing
DrugJune 16, 2014· Baxter Healthcare Corp.

Recalled Item: Brevibloc Premixed Injection Recalled by Baxter Healthcare Corp. Due to...

The Issue: Presence of Particulate Matter: Complaints received of discolored solution...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 16, 2014· Nidek Inc

Recalled Item: Non-Mydriatic Auto Fundus Camera. Model AFC-330. An ophthalmic camera for...

The Issue: Image taken by AFC-330 has a white spot which may affect diagnosis or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2014· McKesson Technologies, Inc.

Recalled Item: Paragon Laboratory Management Recalled by McKesson Technologies, Inc. Due to...

The Issue: For Paragon Laboratory Management 12.1 and 12.1.1 releases, if used with...

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

Class II — Potential Health HazardOngoing
FoodJune 13, 2014· Schnucks Markets Inc

Recalled Item: Schnucks Bakery 8" Devil's Food Cake Recalled by Schnucks Markets Inc Due to...

The Issue: The product contains pecan pieces as a top garnish and the product label...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 13, 2014· Vita Food Products, Inc.

Recalled Item: Vita Classic Premium Sliced Smoked Atlantic Nova Salmon Recalled by Vita...

The Issue: This voluntary recall is being initiated due to a positive Listeria...

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

Class I — Serious Health HazardOngoing
Refund