Product Recalls in Washington

Product recalls affecting Washington — including food, drugs, consumer products, medical devices, and vehicles distributed to Washington. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,058 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
1,058 in last 12 months

Showing 21261–21280 of 51,768 recalls

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
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 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: 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: 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.

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

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Hologic, Inc

Recalled Item: Panther Fusion Extraction Reagent-S Recalled by Hologic, Inc Due to Reagent...

The Issue: Reagent component included in flu test kit may cause both high background...

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: TM Ankle and Ankle Talus L/R 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: Metasul Taper Liner 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 Surgical Instruments: Screws and Reamers 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: 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: 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: 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: 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: 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.

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

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.

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

Recalled Item: Coorad Morrey Total Elbow 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 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