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 26661–26680 of 27,451 recalls
Recalled Item: Extraneal and/or DIANEAL LOW CALCIUM Peritoneal Dialysis Solution in Plastic...
The Issue: Baxter discovered that a Baxter technical service representative was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ABL software version 6.12 for the ABL800 and ABL700 Recalled by...
The Issue: A customer has reported an error on an ABL8xx configured to a Hospital...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 FLEX software version 2.7 MR3. The ABL90 FLEX analyzer Recalled by...
The Issue: A customer has reported an error on an ABL8xx configured to a Hospital...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ABL software version 6.12 for the ABL800 analyzer. The Recalled by...
The Issue: A customer has reported an error on an ABL8xx configured to a Hospital...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes(R) Hemostatic Bone Putty Recalled by Synthes USA HQ, Inc. Due to...
The Issue: There is the potential for Hemostatic Bone Putty to ignite if contacted with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aviator Drill Bit (10 mm Recalled by Stryker Spine Due to Aviator drill bits...
The Issue: Aviator drill bits are 10 mm longer than the Hybrid drill bits and are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTRA Fabric Reinforced surgical Gown X-Large Sterile The product is...
The Issue: Package seam of some units may not remain properly sealed to ensure the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroCool Breathable Gown with Towels Recalled by Kimberly-Clark Corporation...
The Issue: Package seam of some units may not remain properly sealed to ensure the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BP7561 OPTI CCA-TS B-Lac Cassette (25 per box) Cassettes are Recalled by...
The Issue: The values reported for PCO2 by BP7561 B-Lac cassettes are biased at high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fona Srl IntraOs 70 intra-oral x-ray system IntraOS 70 is Recalled by...
The Issue: The IntraOs 70 system was found to have missing or incomplete system labels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffman LRF Telescopic Strut Short Stryker Stryker Trauma AG CH-2545...
The Issue: Three complaints have been filed where the Hoffman LRF Telescopic Struts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with three #2 sutures (white...
The Issue: Distal part of the anchor may break on insertion into bone during surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verify¿ Bowie-Dick Test Card Recalled by Steris Corporation Due to STERIS...
The Issue: STERIS has learned that the Verify Bowie Dick Test Cards are not performing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with two #2 sutures...
The Issue: Distal part of the anchor may break on insertion into bone during surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with two #2 sutures(white...
The Issue: Distal part of the anchor may break on insertion into bone during surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew 5.5 mm TWINFIX Ultra Ti Suture Anchor Recalled by Smith &...
The Issue: Distal part of the anchor may break on insertion into bone during surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPIDER Surgical Instrument: Flexible Clip Applier The SPIDER¿ Surgical...
The Issue: Some clip applier units may be inadequate to achieve clip closure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3mL 9NC Coagulation Sodium Citrate 3.2% Recalled by Greiner Bio-One North...
The Issue: Part of the lot received a lower concentration of citrate solution which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varian brand Varian ARIA Oncology Information System Recalled by Varian...
The Issue: A software anomaly has been identified with the Import Export Application...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bella Blanket Protective Coverlet Recalled by Beekley Corporation Due to...
The Issue: Imaging artifact can occur on mammogram result
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.