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. 2,655 recalls have been distributed to District of Columbia in the last 12 months.
Showing 2101–2120 of 27,451 recalls
Recalled Item: Medline procedure kits labeled as: 1) ANGIO PACK Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) L S GYN PACK Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) C SECTION Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) BREAST PACK-LF Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) ANGIO DRAPE PACK (DRLUL)-LF Recalled...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) EYE PACK Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) C SECTION Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Candida ID Antigen Recalled by Immuno-Mycologics, Inc Due to Candida...
The Issue: Candida Immunodiffusion Antigen may have reduced sensitivity which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Origin Data Management software versions 3.1.0 Recalled by Brainlab AG Due...
The Issue: Under certain circumstances, it can occur that patient records from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon Custom Pak with Non-Latex Symbol Recalled by Alcon Research LLC Due to...
The Issue: Customer-designed sterile surgical procedure packs contain latex components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardiFocus Heartlight X3 Catheter- Intended in the treatment of atrial...
The Issue: Damage to the sterile barrier pouch of catheter, which could potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DR DIULUS INJECTION PACK Recalled by American Contract Systems Inc Due to...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LABOR & DELIVERY PPS Recalled by American Contract Systems Inc Due to ACS is...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline ReNewal Reprocessed Livewire Steerable Electrophysiology Catheters...
The Issue: Devices may have higher than expected amounts of bacterial endotoxin.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAJOR VASCULAR PACK Recalled by American Contract Systems Inc Due to ACS is...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LABOR & DELIVERY PACK Recalled by American Contract Systems Inc Due to ACS...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CENTRAL LINE PICC Recalled by American Contract Systems Inc Due to ACS is...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DIAGNOSTIC NEURO IR TRAY Recalled by American Contract Systems Inc Due to...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GENERAL LAPAROSCOPIC PACK-LF Recalled by American Contract Systems Inc Due...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-SECTION PACK Recalled by American Contract Systems Inc Due to ACS is...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.