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. 1,737 recalls have been distributed to District of Columbia in the last 12 months.
Showing 32781–32800 of 47,654 recalls
Recalled Item: TM CR TIB SZ 3 C-H Recalled by Zimmer Trabecular Metal Technology, Inc. Due...
The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REV. SHELL LINER 0D 28X48 00700504828 REV. SHELL LINER 10D Recalled by...
The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POROUS PATELLA 32MM X 10MM - 00587806532 POROUS PATELLA 35MM Recalled by...
The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00720504022 ACETAB.CUPW/SH Recalled by Zimmer Trabecular Metal Technology,...
The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to Potential...
The Issue: Potential non-recoverable loss of image acquisition. The affected Discovery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to Potential...
The Issue: Potential non-recoverable loss of image acquisition. The affected Discovery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Given Imaging Bravo¿ pH capsule delivery device Recalled by Covidien LLC Due...
The Issue: Potential of an allergic reaction in a patient with nickel sensitivity.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Given Imaging Bravo¿¿ pH capsule delivery device Recalled by Covidien LLC...
The Issue: Potential of an allergic reaction in a patient with nickel sensitivity.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESTREAM Image Suite V3: MINI-PACS/F IMG ST/CLASSIC: REF/Catalog # 1036490...
The Issue: Carestream Health received a complaint related to CARESTREAM Image Suite 4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEXL-3010/A5- Vantage Titan 3T Magnetic Resonance Imaging System Product...
The Issue: A potential problem associated to the gradient coil (ASGC) in the Titan 3T...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo Dynamics Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens has identified changes in default carry forward workflow using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentaray NAV High-Density Mapping Catheter Recalled by Biosense Webster,...
The Issue: Biosense Webster is recalling the Pentaray Catheters to clarify the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CytoScan¿ Dx Assay. The CytoScan Dx Assay consists of five reagent modules...
The Issue: During a recent Ohio site inspection by the FDA it was discovered that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentaray NAV High-Density Mapping ECO Catheter Recalled by Biosense Webster,...
The Issue: Biosense Webster is recalling the Pentaray Catheters to clarify the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magnesium on RX Imola analyser IVD Recalled by Randox Laboratories, Limited...
The Issue: According to the firm, Carry over was observed when the amylase or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-Vented Dispensing Pin with One-Way Valve and Luer Lock Ultrasite...
The Issue: BBMI recently identified a potential for a tear in the outer blister...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-Vented Dispensing Pin with Luer Lock Ultrasite Valve Product Usage:...
The Issue: BBMI recently identified a potential for a tear in the outer blister...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4 GL PAIL FRUIT MIX-SMALL CUT Recalled by Simply Fresh Fruit Due to...
The Issue: Simply Fresh Fruit is recalling cantaloupe and fruit mixes with cantaloupe...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 4/1 GL CANT/HONEYDEW/PINEAPPLE 3/4" Recalled by Simply Fresh Fruit Due to...
The Issue: Simply Fresh Fruit is recalling cantaloupe and fruit mixes with cantaloupe...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 2/1 GL SYSCO IMP. FRUIT MIX -LS Recalled by Simply Fresh Fruit Due to...
The Issue: Simply Fresh Fruit is recalling cantaloupe and fruit mixes with cantaloupe...
Recommended Action: Do not consume. Return to store for a refund or discard.