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. 2,448 recalls have been distributed to District of Columbia in the last 12 months.
Showing 27221–27240 of 47,654 recalls
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pravastatin Sodium Tablets Recalled by International Laboratories, Inc. Due...
The Issue: Labeling: Label mix-up, the product labeled as Pravastatin sodium tablets 40...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Michele s Toasted Muesli Recalled by Michele's Granola LLC Due to Potential...
The Issue: The product has been recalled due to the potential to be contaminated with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Merge Unity software Recalled by Merge Healthcare, Inc. Due to The software...
The Issue: The software is not identifying the patient as having atypical hyperplasia,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Cemented Tibial SZ PLT Size H Left Recalled by Zimmer Biomet, Inc....
The Issue: There is a potential for intermittent cracks in the raw material batch used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Cemented Tibial SZ PLT Size H Right Recalled by Zimmer Biomet, Inc....
The Issue: There is a potential for intermittent cracks in the raw material batch used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Stemmed Tibial Provisional Size H Right Recalled by Zimmer Biomet,...
The Issue: There is a potential for intermittent cracks in the raw material batch used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Stemmed Tibial Provisional Size H Left Recalled by Zimmer Biomet,...
The Issue: There is a potential for intermittent cracks in the raw material batch used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quillivant XR methylphenidate HCl Recalled by Pfizer Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Quillivant XR methylphenidate HCl Recalled by Pfizer Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to The barcode...
The Issue: The barcode label was placed underneath the sterile barrier and the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to The barcode...
The Issue: The barcode label was placed underneath the sterile barrier and the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to The barcode...
The Issue: The barcode label was placed underneath the sterile barrier and the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to The barcode...
The Issue: The barcode label was placed underneath the sterile barrier and the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OneStep CPR Complete Recalled by ZOLL Medical Corporation Due to A portion...
The Issue: A portion of one lot of ZOLL OneStep Complete Electrodes for adults will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to The barcode...
The Issue: The barcode label was placed underneath the sterile barrier and the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Response 5.5/6.0 Spine System 7.0mm x 40mm Pedicle Screw Product Recalled by...
The Issue: The 7mm diameter uniaxial pedicle screws have been color anodized with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitamin A&D Ointment (petroleum 93.5%) Recalled by MEDLINE INDUSTRIES INC...
The Issue: Labeling Mixup; the individual A&D ointment foil packets are incorrectly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phentermine HCL Capsules Recalled by KVK-Tech, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lorazepam Oral Concentrate Recalled by Amneal Pharmaceuticals of New York,...
The Issue: Defective Delivery System: the dropper measurement markings may be reversed,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.