Product Recalls in Arizona

Product recalls affecting Arizona — including food, drugs, consumer products, medical devices, and vehicles distributed to Arizona. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,600 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,600 in last 12 months

Showing 2104121060 of 52,339 recalls

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
Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: Metasul 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: DIST LAT FEM LCK PLATE 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: Various Devices for Limb salvage 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: PERIARTICULAR PLATES SHOULDER 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: NCB-PH Plate with 4/5/7 Lock Holes 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: NCB Straight Narrow 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: 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: 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.

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· Trilliant Surgical, LLC

Recalled Item: 3.5mm Aresenal Screw Drill Bit Recalled by Trilliant Surgical, LLC Due to...

The Issue: Labeling Error; specifically, drill bits from lots # TSL008495A are marked...

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: Cephalomedullary Nail (CMN) 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: cable button for NCB¿ Polyaxial Locking Plate 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
FoodOctober 10, 2019· Dollar General Corporation

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.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 9, 2019· Medivators, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Medivators, Inc.

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.

Class II — Potential Health HazardOngoing