Product Recalls in Colorado
Product recalls affecting Colorado — including food, drugs, consumer products, medical devices, and vehicles distributed to Colorado. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,563 recalls have been distributed to Colorado in the last 12 months.
Showing 18901–18920 of 28,964 recalls
Recalled Item: Biograph 6 TruePoint Recalled by Siemens Medical Solutions USA Inc. Due to...
The Issue: The mobile-specific instructions was not shipped to a limited population of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to Software...
The Issue: Software updates
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soft Face "No Bounce" Mallet Model/Catalog: BIO-1-1090 Recalled by Signal...
The Issue: Potential for poly tip of the mallet to come off during use. Potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: various polyethylene implants Hips Active Articulation ArComXL Bearings...
The Issue: Endotoxin levels higher than process maximum limits were discovered in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: various polyethylene implants Extremities Recalled by Zimmer Biomet, Inc....
The Issue: Endotoxin levels higher than process maximum limits were discovered in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: various polyethylene implants Custom parts Product Usage: Custom Recalled by...
The Issue: Endotoxin levels higher than process maximum limits were discovered in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: various polyethylene implants BIO PLUG 10MM Product Usage: Non-weight...
The Issue: Endotoxin levels higher than process maximum limits were discovered in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: various polyethylene implants Sports Med Repicci II Tibial Components...
The Issue: Endotoxin levels higher than process maximum limits were discovered in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: various polyethylene implants Knees Revision Tibial Tray Systems Oxford...
The Issue: Endotoxin levels higher than process maximum limits were discovered in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7F Prelude¿ Short Sheath Introducer. Catalog Numbers: K15-00070 Recalled by...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for sheaths...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MotoCLIP(TM) Super Elastic Fusion System Recalled by Crossroads Extremity...
The Issue: Seven 18mm x 18mm x 18 mm implants had been placed in kits, packed and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Miriam Capsule Endoscope System. Model MR1100 Product Usage: MiroCam Capsule...
The Issue: When a user switches on MR1100 Receiver, even though the battery was fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit. Dialyzer Recalled by Baxter Healthcare Corporation...
The Issue: Firm has received reports of device operators failing to adhere to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthosize Templating Version 1.2.6 Echo Bi-Metric Hip Stem Digital...
The Issue: Digital templates were created with the incorrect files.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modera Modular Pedicle Screw System Shank Insertion Instrument Recalled by...
The Issue: This is a retrospective recall of an instrument used in spine fusion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus ENDOEYE HD II Video Telescopes Models: WA50040A Endoeye HD II...
The Issue: A damaged temperature sensor at the endoscope's tip can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bivona¿ TTS (Tight to Shaft) Pediatric Tracheostomy Tube Recalled by Smiths...
The Issue: Smiths Medical became aware that one lot of the Bivona¿ 3.5mm TTS Cuffed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ViperWire Advance with Flextip Peripheral Atherectomy Guide Wire Recalled by...
The Issue: CSI is recalling three lots of VIPERWIRE ADVANCE WITH FLEXTIP PERIPHERAL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Recalled by Remel Inc Due to Test organisms exhibit poor growth when...
The Issue: Test organisms exhibit poor growth when grown using the test agar. The poor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arkon Anesthesia Delivery System Recalled by Del Mar Reynolds Medical, Ltd....
The Issue: Spacelabs has received reports of the Arkon Anesthesia Delivery System,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.