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. 1,713 recalls have been distributed to District of Columbia in the last 12 months.
Showing 41201–41220 of 47,654 recalls
Recalled Item: Device Name: ABX PENTRA ML Model/Part #(s): A11A01652 Lot/Serial #(s):...
The Issue: HORIBA Medical initiated this recall of all software versions of ABX PENTRA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluoxetine Capsules Recalled by Legacy Pharmaceutical Packaging Due to...
The Issue: Chemical Contamination: The recalling firm received notice that their...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: etomidate injection Recalled by Agila Specialties Private Ltd. Due to...
The Issue: Presence of Particulate Matter: Potential for small black particles to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetylcysteine Solution Recalled by Ben Venue Laboratories Inc Due to...
The Issue: Presence of Particulate Matter: During a review of retain samples, the firm...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CITRULLINE (L) in 25 g Recalled by Medisca Inc Due to Labeling: Label...
The Issue: Labeling: Label Mix-Up: FDA tested samples of API from Medisca, labeled as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GE Healthcare Solar 8000M and Solar 8000i Patient Monitor software version...
The Issue: GE Healthcare has recently become aware of a potential safety issue with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VerifyNow IIb/IIIa Test Recalled by Accumetrics Inc Due to Accumetrics is...
The Issue: Accumetrics is recalling the VerifyNow IIb/IIIa test because it may result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Other Macaroon G'nache P'nache 5.3 oz. Manufactured and Distributed...
The Issue: Northern Valley Baking Company did not declare milk or soy on the allergen...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluoxetine Capsules USP Recalled by Teva Pharmaceuticals USA Due to Chemical...
The Issue: Chemical Contamination: Recall due to a customer complaint trend regarding...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluoxetine Capsules USP Recalled by Teva Pharmaceuticals USA Due to Chemical...
The Issue: Chemical Contamination: Recall due to a customer complaint trend regarding...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ARCHITECT Intact PTH Calibrators consists of 6 bottles (4.0 mL Recalled by...
The Issue: Abbott has confirmed that a performance shift in the ARCHITECT Intact PTH...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT Intact PTH Controls consists of 3 x 1 Bottle Recalled by Abbott...
The Issue: Abbott has confirmed that a performance shift in the ARCHITECT Intact PTH...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Synthes Hohmann Retractor Recalled by Synthes, Inc. Due to The Synthes...
The Issue: The Synthes Hohmann Retractor was mis-etched on the product and package as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS URIC ACID For the In vitro quantitative determination of Recalled by AMS...
The Issue: Marketing the devices outside 510(k) requirements
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS AST For the In vitro quantitative determination of AST Recalled by AMS...
The Issue: Marketing the devices outside 510(k) requirements
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS BUN UREA NITROGEN For the In vitro quantitative determination Recalled...
The Issue: Marketing the devices outside 510(k) requirements
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Ventilators The Respironics Trilogy 100 system provides continuous...
The Issue: Internal testing revealed a potentially defective component on the power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinnacle3 Radiation Therapy Planning (RTP) System Recalled by Philips...
The Issue: Philips Medical Systems have recently determined that a software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.