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. 2,395 recalls have been distributed to District of Columbia in the last 12 months.
Showing 42101–42120 of 47,654 recalls
Recalled Item: Human Chorionic Gonadotropin Recalled by Medisca Inc. Due to Labeling: Label...
The Issue: Labeling: Label Error on Declared Strength; Firm states that erroneous...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SuperDigestZyme (Z22) Recalled by Apex Energetics Due to Apex Energetics is...
The Issue: Apex Energetics is recalling GlutenFlam, SuperDigestZyme, LGS-Zyme, and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RepairVite (K63) Recalled by Apex Energetics Due to Apex Energetics is...
The Issue: Apex Energetics is recalling GlutenFlam, SuperDigestZyme, LGS-Zyme, and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GlutenFlam (K-52) Enzyme & Bioflavonoid Dietary Supplement Recalled by Apex...
The Issue: Apex Energetics is recalling GlutenFlam, SuperDigestZyme, LGS-Zyme, and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: LGS-Zyme (Z12) Recalled by Apex Energetics Due to Apex Energetics is...
The Issue: Apex Energetics is recalling GlutenFlam, SuperDigestZyme, LGS-Zyme, and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: THUNDER¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COUGAR¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProVia¿ CROSSING GUIDEWIRE Recalled by Medtronic Vascular Due to Potential...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZINGER¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTAIN HYBRID¿ Guide Wire Recalled by Medtronic Vascular Due to Potential...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THUNDER¿ Extra Support Guidewire Recalled by Medtronic Vascular Due to...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zinger¿ Stainless Steel Workhorse Guidewire Recalled by Medtronic Vascular...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cougar¿ Nitinol Workhorse Guidewire: Models: CGRLS190HJ Recalled by...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Applied Medical's Inzii¿ 12/15mm Retrieval System. Applieds Inzii Tissue...
The Issue: Applied Medical is conducting a voluntary recall of the Inzii¿ 12/15mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prostiva RF Therapy Hand Piece Kit Recalled by Urologix, Inc. Due to A Hand...
The Issue: A Hand Piece high deployment force exceeded the maximum specification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VitreaCore¿ software. Versions subject to the limitation: 6.0 Recalled by...
The Issue: Vital Images, Inc. has found an issue in VitreaCore software though internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Vision System Cart Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Intuitive has identified that the metalized coating on the IS3000 HD lamp...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Marcaine (bupivacaine HCl) injection Recalled by Hospira Inc. Due to...
The Issue: Presence of Particulate Matter: Units of this lot may have visible metal...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CRN Crono Syringe CRN20 with 19G x 1 "Steel Needle" Recalled by Intra Pump...
The Issue: Product has the potential to have a clear debris on the tip of the needle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSCO¿ Evolution¿ steam sterilizer Transfer Carriage. Product Usage: Mobile...
The Issue: The firm discovered that unlatching can occur when overloaded transfer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.