Product Recalls in District of Columbia

Product recalls affecting District of Columbia — including food, drugs, consumer products, medical devices, and vehicles distributed to District of Columbia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,411 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,411 in last 12 months

Showing 3916139180 of 47,654 recalls

Medical DeviceNovember 11, 2014· Heart Sync, Inc.

Recalled Item: ADULT Radiotranslucent Electrode Recalled by Heart Sync, Inc. Due to Heart...

The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 11, 2014· Cure Medical LLC

Recalled Item: Pediatric Recalled by Cure Medical LLC Due to Some of the intermediate boxes...

The Issue: Some of the intermediate boxes within lot 140417-3, were labeled as P8, a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2014· Ebi, Llc

Recalled Item: Solitaire-C Cervical Spacer System a) 14-531593 Drill/Awl Sleeve b)...

The Issue: A design deficiency was discovered whereby the Drill/Awl Sleeve and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2014· Heart Sync, Inc.

Recalled Item: ADULT Radiotransparent Electrode Recalled by Heart Sync, Inc. Due to Heart...

The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 11, 2014· Heart Sync, Inc.

Recalled Item: ADULT/CHILD Radiotranslucent Electrode Recalled by Heart Sync, Inc. Due to...

The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 11, 2014· Heart Sync, Inc.

Recalled Item: ADULT/CHILD Radiotransparent Electrode Recalled by Heart Sync, Inc. Due to...

The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 11, 2014· Vision Rt Inc

Recalled Item: AlignRT is a video-based three-dimensional (3D) surface imaging system which...

The Issue: Potential use error when the external Gate Controller is turned ON after...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to Printouts...

The Issue: Printouts may be printed in incorrect anatomical size when using syngo.plaza...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2014· Alcon Research, Ltd.

Recalled Item: Alcon Single-Use Curved Jewelers/Iris Bipolar Forceps Sterile RX Recalled by...

The Issue: The product is sold and labeled as EO sterilized, however the units were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2014· Heart Sync, Inc.

Recalled Item: ADULT Radiotranslucent Electrode Recalled by Heart Sync, Inc. Due to Heart...

The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...

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

Class I — Serious Health HazardOngoing
FoodNovember 11, 2014· InHarvest, Inc.

Recalled Item: Rio Medley/Garden Vegetable 12/36 oz Recalled by InHarvest, Inc. Due to Firm...

The Issue: Firm was notified by supplier of Garden Vegetable Seasoning that the product...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 11, 2014· InHarvest, Inc.

Recalled Item: White and Wild Medley/Garden Vegetable 12/36 oz Recalled by InHarvest, Inc....

The Issue: Firm was notified by supplier of Garden Vegetable Seasoning that the product...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 11, 2014· InHarvest, Inc.

Recalled Item: Garden Vegetable seasoning Mix 12/4 oz. Product number 141000 Garden...

The Issue: Firm was notified by supplier of Garden Vegetable Seasoning that the product...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 11, 2014· InHarvest, Inc.

Recalled Item: Whole Grain 5 Blend/Garden Vegetable 12/36 oz Product number 12410 Recalled...

The Issue: Firm was notified by supplier of Garden Vegetable Seasoning that the product...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 11, 2014· InHarvest, Inc.

Recalled Item: Caviar Medley/Garden Vegetable 12/36 oz Product number 10610 Recalled by...

The Issue: Firm was notified by supplier of Garden Vegetable Seasoning that the product...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 10, 2014· Baxter Healthcare Corp.

Recalled Item: Potassium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...

The Issue: Labeling: Label Error On Declared Strength: Bags of Potassium Chloride 10...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 10, 2014· Reckitt Benckiser LLC

Recalled Item: Mucinex DM (guaifenesin 600mg and dextromethorphan HBr 30mg) Recalled by...

The Issue: Defective container: A customer complaint revealed the presence of a...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 10, 2014· DePuy Orthopaedics, Inc.

Recalled Item: Fixed Tibial bearing ATTUNE INTUITION Impactor The ATTUNE INTUITION...

The Issue: ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006)...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2014· DePuy Orthopaedics, Inc.

Recalled Item: Femoral Impactor ATTUNE INTUITION Impactor. The ATTUNE INTUITION Impactors...

The Issue: ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006)...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2014· DePuy Orthopaedics, Inc.

Recalled Item: Rotating Tibial Platform ATTUNE INTUITION Impactor. The ATTUNE INTUITION...

The Issue: ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006)...

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

Class II — Potential Health HazardOngoing