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. 2,472 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,472 in last 12 months

Showing 2390123920 of 47,654 recalls

Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-MP60 Recalled by Olympus Corporation of the Americas...

The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-1T180 Recalled by Olympus Corporation of the Americas...

The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchofiberscope BF-40 Recalled by Olympus Corporation of the Americas Due...

The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-1T40 Recalled by Olympus Corporation of the Americas...

The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovidescope BF-1T240 Recalled by Olympus Corporation of the Americas...

The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-P160 Recalled by Olympus Corporation of the Americas...

The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-3C160 Recalled by Olympus Corporation of the Americas...

The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...

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

Class II — Potential Health HazardOngoing
DrugAugust 7, 2018· Mylan Pharmaceuticals Inc.

Recalled Item: Diltiazem HCl Extended-Release Capsules Recalled by Mylan Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: Out of specification test...

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

Class III — Low RiskOngoing
Refund
DrugAugust 7, 2018· Mylan Pharmaceuticals Inc.

Recalled Item: Diltiazem HCl Extended-Release Capsules Recalled by Mylan Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: Out of specification test...

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

Class III — Low RiskOngoing
Refund
DrugAugust 7, 2018· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Doxycycline Hyclate USP Tablets Recalled by PD-Rx Pharmaceuticals, Inc. Due...

The Issue: Failed Dissolution Specifications: manufacturer West-Ward Pharm Corp....

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 7, 2018· Natures Bounty Inc

Recalled Item: BLUE GREEN ALGAE: Packaged under the following brands: AMERICAN HEALTH...

The Issue: High level of microcystin observed in the product.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 7, 2018· Medtronic Inc.

Recalled Item: Minimed Model 503 Remote Transmitter (MMT-503 Recalled by Medtronic Inc. Due...

The Issue: There is a potential security vulnerability related to the use of the remote...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 7, 2018· Medtronic Inc.

Recalled Item: Minimed Model 500 Remote Control (MMT-500 Recalled by Medtronic Inc. Due to...

The Issue: There is a potential security vulnerability related to the use of the remote...

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

Class I — Serious Health HazardOngoing
FoodAugust 6, 2018· Country Favor Inc.

Recalled Item: BEST TASTE BRAND SNACK GINGER SLICED Recalled by Country Favor Inc. Due to...

The Issue: Product contains high levels of undeclared sulfites.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 6, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Ysio MAX (model number 10762470) with Tube stand 3D V Recalled by Siemens...

The Issue: In rare cases of high clinical workload, the steel cables inside the lifting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Ysio (model number 10281013 or 10281163) with Tube stand 3D Recalled by...

The Issue: In rare cases of high clinical workload, the steel cables inside the lifting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Multix MT (model number 8395415 or 8395399 or 8395381) Recalled by...

The Issue: In rare cases of high clinical workload, the steel cables inside the lifting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2018· Dannoritzer Medizintechnik GmbH & Co. KG

Recalled Item: Laparoscopy Instruments Instructions For Use (IFU) for the following:...

The Issue: The Manual cleaning process and the usability of the reprocessing...

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

Class III — Low RiskOngoing
DrugAugust 3, 2018· Product Quest Manufacturing LLC

Recalled Item: Rhinall (phenylephrine hydrochloride) Nasal Decongestant Nose Drops Recalled...

The Issue: CGMP Deviations: products manufactured under conditions that could impact...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 3, 2018· Product Quest Manufacturing LLC

Recalled Item: CVS Health Recalled by Product Quest Manufacturing LLC Due to CGMP...

The Issue: CGMP Deviations: products manufactured under conditions that could impact...

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

Class II — Potential Health HazardOngoing
Refund