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. 2,485 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,485 in last 12 months

Showing 2096120980 of 47,654 recalls

FoodJuly 11, 2019· Wismettac Asian Foods, INC

Recalled Item: Shirakiku FISH CAKE OHBAN AGE SK F Recalled by Wismettac Asian Foods, INC...

The Issue: Fish Cake items contain possible contaminating undeclared egg, milk and...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 11, 2019· Wismettac Asian Foods, INC

Recalled Item: Shirakiku FISH CAKE SATSUMA AGE SK F Recalled by Wismettac Asian Foods, INC...

The Issue: Fish Cake items contain possible contaminating undeclared egg, milk and...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 11, 2019· Wismettac Asian Foods, INC

Recalled Item: Shirakiku FISH CAKE IWASHI TEN SK F 20/150 g Recalled by Wismettac Asian...

The Issue: Fish Cake items contain possible contaminating undeclared milk and shellfish.

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 11, 2019· Wismettac Asian Foods, INC

Recalled Item: Shirakuku FISH CAKE MINCH BALL SK F Recalled by Wismettac Asian Foods, INC...

The Issue: Fish Cake items contain possible contaminating undeclared egg, milk and...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 11, 2019· Merge Healthcare, Inc.

Recalled Item: Merge OrthoPACS versions 7.3 Recalled by Merge Healthcare, Inc. Due to...

The Issue: Potential for prior thumbnails to not display in reverse chronological order...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2019· Merge Healthcare, Inc.

Recalled Item: Merge PACS versions 7.3 Recalled by Merge Healthcare, Inc. Due to Potential...

The Issue: Potential for prior thumbnails to not display in reverse chronological order...

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

Class II — Potential Health HazardOngoing
DrugJuly 10, 2019· LNK International, Inc.

Recalled Item: Equate Night-time Sleep Aide (Diphenhydramine HCl) Recalled by LNK...

The Issue: Microbial contamination of non-sterile product

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 10, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 1000 Progesterone Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: There is a potential for low discordant progesterone results on a subset of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 Progesterone Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: There is a potential for low discordant progesterone results on a subset of...

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

Class II — Potential Health HazardOngoing
DrugJuly 9, 2019· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Drospirenone and Ethinyl Estradiol Tablets Recalled by Jubilant Cadista...

The Issue: Failed dissolution specifications : failed results at the 3-month stability...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 9, 2019· Probar LLC

Recalled Item: PROBAR MEAL Superfood Slam Recalled by Probar LLC Due to Undeclared Milk

The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 9, 2019· Probar LLC

Recalled Item: PROBAR The Simply Real Bar: Chocolate Coconut Recalled by Probar LLC Due to...

The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 9, 2019· Probar LLC

Recalled Item: PROBAR MEAL Original Trail Mix Recalled by Probar LLC Due to Undeclared Milk

The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 9, 2019· Probar LLC

Recalled Item: PROBAR MEAL Peanut Butter Chocolate Chip Recalled by Probar LLC Due to...

The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 9, 2019· Probar LLC

Recalled Item: PROBAR MEAL Chocolate Coconut Recalled by Probar LLC Due to Undeclared Milk

The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 9, 2019· Probar LLC

Recalled Item: PROBAR MEAL Wholeberry Blast Recalled by Probar LLC Due to Undeclared Milk

The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 9, 2019· Phadia Ab

Recalled Item: Phadia" 1000 Model # 12-3800-01 Product Usage: The instrument is Recalled by...

The Issue: code 7-102 Liquid Sensor Error

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Spectra magnetic resonance diagnostic devices Model # 10837643...

The Issue: Potential of an open port in the quench venting system when using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Prisma magnetic resonance diagnostic devices Model #10849582...

The Issue: Potential of an open port in the quench venting system when using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Skyra magnetic resonance diagnostic devices Model # 10432915...

The Issue: Potential of an open port in the quench venting system when using the...

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

Class II — Potential Health HazardOngoing