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. 1,035 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
1,035 in last 12 months

Showing 30081–30100 of 55,602 recalls

Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: VERSYS 10 INCH BEADED FC REV 13.5X250MM BWD LT and Recalled by Zimmer...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: CR-FLEX OPT FEM C-L CR-FLEX OPT FEM C-R CR-FLEX OPT Recalled by Zimmer...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: LCCK FEM IMPLANT SZ C-L LCCK FEM IMPLANT SZ C-R Recalled by Zimmer Biomet,...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: CPT 12/14 COCR SIZE 2 STD prosthesis Recalled by Zimmer Biomet, Inc. Due to...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: CR-FLEX PCT FEM B-R CR-FLEX PCT FEM C-L CR-FLEX PCT Recalled by Zimmer...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: VERSYS 6 INCH BEADED FC 12X160MM LM BODY EXT NECK Recalled by Zimmer Biomet,...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: LPS FEM COMP SZ B-L LPS FEM COMP SZ B-R Recalled by Zimmer Biomet, Inc. Due...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: CR-FLX POR HATCP FEM C-L MINUS CR-FLX POR HATCP FEM Recalled by Zimmer...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodNovember 28, 2017· JP's Delicacies LLC

Recalled Item: Holi Aioli Recalled by JP's Delicacies LLC Due to JP s Delicacies LLC of...

The Issue: JP s Delicacies LLC of Bloomfield NJ discovered during a walk thru of area...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 28, 2017· Teva Pharmaceuticals USA

Recalled Item: Penicillin V Potassium for Oral Solution Recalled by Teva Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: high out of specification test...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugNovember 28, 2017· EAI-JR286 INC

Recalled Item: Vertra Elemental Resistance (Octyl Methoxycinnamate 6% Recalled by EAI-JR286...

The Issue: CGMP Deviations: products manufactured in a manner that may impact product...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 27, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Syva¿ EMIT¿ 2000 Theophylline Product Usage: The Syva¿ Emit¿ 2000 Recalled...

The Issue: Lot J1 of the Syva¿ EMIT¿ 2000 Theophylline Assay, when run on a Beckman AU...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Cincinnati Sub-Zero Products LLC

Recalled Item: Hemotherm¿ Dual Reservoir Cooler/Heater System Models 400CE and 400MR...

The Issue: Due to FDA's safety communication relating to nontuberculous mycobacteria...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Ethicon, Inc.

Recalled Item: DERMABOND" PRINEO" Skin Closure System Product Usage: DERMABOND PRINEO...

The Issue: Ethicon discovered that specific lots of DERMABOND"PRINEO"System may not dry...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodNovember 27, 2017· H. A. R. Maspeth Corp.

Recalled Item: WOLDONG WORLD'S BEST KIMCHI WHOLE CABBAGE KIMCHI PREMIUM 3LBS (1.36kg)...

The Issue: Product contains undeclared sesame seeds.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 21, 2017· Lupin Pharmaceuticals Inc.

Recalled Item: Duloxetine Delayed-Release Capsules USP Recalled by Lupin Pharmaceuticals...

The Issue: Failed Dissolution Specification

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 21, 2017· Covidien LLC

Recalled Item: Rechargeable Li-ion battery used with Puritan Bennett TM 980 Series Recalled...

The Issue: Rechargeable lithium-ion batteries with incorrect firmware that are used in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2017· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: 10 ML REAGENT CUP Recalled by Horiba Instruments, Inc dba Horiba Medical Due...

The Issue: The ABX PENTRA Reagent Containers do not always sit properly into the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2017· SANTA JOY ORNAMENT & GIFTWARE CO

Recalled Item: Santajoy Ornament & Giftware Co. Recalled by SANTA JOY ORNAMENT & GIFTWARE...

The Issue: It was discovered that the product units it imported may, at peak levels,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2017· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: 15 ML REAGENT CUP Recalled by Horiba Instruments, Inc dba Horiba Medical Due...

The Issue: The ABX PENTRA Reagent Containers do not always sit properly into the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing