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. 2,547 recalls have been distributed to District of Columbia in the last 12 months.
Showing 18081–18100 of 47,654 recalls
Recalled Item: STAT KIT Model 550 Emergency Medical Kit P/N: 1009580 containing Recalled by...
The Issue: Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAT KIT Recalled by HF Acquisition Co., LLC Due to Instead of 2 doses,...
The Issue: Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HealthFirst Emergency Medical Kit Recalled by HF Acquisition Co., LLC Due to...
The Issue: Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...
The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...
The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...
The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...
The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...
The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...
The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...
The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...
The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...
The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...
The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health NPWT Canister with Gel 300cc Recalled by Cardinal Health...
The Issue: Canisters potentially contain an oversized O-ring that cannot be installed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health NPWT Occlusion Detection Canister 300cc Recalled by Cardinal...
The Issue: Canisters potentially contain an oversized O-ring that cannot be installed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soft Whisper by Powerstick Dandruff Shampoo (Pyrithione Zinc) Recalled by...
The Issue: cGMP Deviations: Soft Whisper Dandruff Shampoo was produced with water that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PrimeStore Molecular Transport Medium (PS-MTM) Recalled by LONGHORN VACCINES...
The Issue: The tubes may have been delivered to some users without labels. Users may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MagNA Pure 96 Instrument Recalled by Roche Molecular Systems, Inc. Due to...
The Issue: When using Sample Transfer protocol version 3.0, the drop catcher is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COOPERSURGICAL Os FinderTM Cervical Dilator Recalled by CooperSurgical, Inc....
The Issue: Mislabeled: Printing on the top web or Tyvek lid of the individual product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow Coupler Monitor Recalled by Baxter Healthcare Corporation Due to A...
The Issue: A firmware issue may cause the GEM1020M-2 Flow Coupler Monitor to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.