Product Recalls in Pennsylvania
Product recalls affecting Pennsylvania — including food, drugs, consumer products, medical devices, and vehicles distributed to Pennsylvania. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,113 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 13301–13320 of 29,947 recalls
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: 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: 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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. . 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: 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.