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. 2,551 recalls have been distributed to Colorado in the last 12 months.
Showing 20881–20900 of 51,434 recalls
Recalled Item: Fitmore Hip Stem Recalled by Zimmer Biomet, Inc. Due to Non-highly polished...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trabecular Metal Reverse Shoulder System Recalled by Zimmer Biomet, Inc. Due...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Hip Joint Replacement Systems Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CABLE-READY SHORT GTR and CABLE-READY LONG GTR Recalled by Zimmer Biomet,...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SM DIS VOL/DORS RAD LAT COL PLATE Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLS Brevius Stem Kinectiv Recalled by Zimmer Biomet, Inc. Due to Non-highly...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FEMOROTIBIAL/FEMORAL NAIL Recalled by Zimmer Biomet, Inc. Due to Non-highly...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sweet Smiles brand Select Dark Chocolate with Orange Peel Bar Recalled by...
The Issue: Possible undeclared milk allergen in product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medivators Endo Smartcap Endoscope Tubing. Recalled by Medivators, Inc. Due...
The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medivators Endo Smartcap Endoscope Tubing. Recalled by Medivators, Inc. Due...
The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medivators EndoGator . Kit for Olympus 140/160/180/190 Series GI Recalled by...
The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medivators EndoGator . Kit for Olympus 140/160/180/190 Series GI Recalled by...
The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medivators Endo carry-on Procedure Kit - Product Usage: Recalled by...
The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Tourniquet Cuff 30" (Blue) Recalled by Stryker Sustainability...
The Issue: Tourniquet cuffs are potentially mislabeled. If used may lead to (1) Device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medivators Endo Smartcap Endoscope Tubing. Recalled by Medivators, Inc. Due...
The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity M300 telemetry monitoring device Software versions VG2.3.1 and...
The Issue: The devices have potential cybersecurity vulnerabilities, which can include...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medivators Endo Smartcap Endoscope Tubing. . Packaged as Contents 1 Recalled...
The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stratum Foot Plating System-NL LP Screw 3.5x50mm ST Recalled by Nextremity...
The Issue: Product labeled as STRM-NL-3550ST, NL LP Screw 3.5x50mm ST, lot M1151 may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PF-Fentanyl Citrate 2 mcg/mL* & Bupivacaine HCl 0.125% in 0.9% Recalled by...
The Issue: GMP Deviations: potential glass contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PF-Fentanyl Citrate 2 mcg/mL* & Ropivacaine HCl 0.1% in 0.9% Recalled by...
The Issue: GMP Deviations: potential glass contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.