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.

51,434 total recalls
2,551 in last 12 months

Showing 2086120880 of 51,434 recalls

Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: Periarticular Plates - Tibial 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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: Various Knee Systems for knee joint arthroplasty 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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: Universal Locking Plates Sterile 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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: ZPLP Fibular Plate 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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: LPS-MOB ART SURF IMPL D 9MM 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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: Various fixation systems and accessories 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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: Periarticulare Plates - Elbow 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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: PROX LAT HUMERAL LOCK 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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: Various fixation systems and accessories 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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: Sidus Stem-Free Shoulder Humeral Head 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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: PERI DIST VOLAR/DORSAL T/DORSAL DELTA RADIAL Recalled by Zimmer Biomet, Inc....

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: Ceramic Femoral Heads 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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: Various temporary devices used during the implantation of the device...

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: NCB PERIPROSTHETIC 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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: Prox Lat Tib Lock Plate and Dist Med Tib Lock 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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: Various Knee Systems 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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: PERIARTICULAR PLATES - FEMUR 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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: Connection Screw for NCB 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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: Periarticular locking plate elbow-sterile Recalled by Zimmer Biomet, Inc....

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: BF Humeral 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.

Class II — Potential Health HazardOngoing