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. 1,064 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
1,064 in last 12 months

Showing 18341–18360 of 55,602 recalls

DrugDecember 23, 2020· Shane Erickson Inc

Recalled Item: IMC Wash-Free Hand Sanitizer Recalled by Shane Erickson Inc Due to CGMP...

The Issue: CGMP Deviations: product manufactured at the same facility that produced...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 23, 2020· Shane Erickson Inc

Recalled Item: IMC Wash-Free Hand Sanitizer Recalled by Shane Erickson Inc Due to CGMP...

The Issue: CGMP Deviations: product manufactured at the same facility that produced...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 23, 2020· Shane Erickson Inc

Recalled Item: IMC Wash-Free Hand Sanitizer Recalled by Shane Erickson Inc Due to CGMP...

The Issue: CGMP Deviations: product manufactured at the same facility that produced...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 23, 2020· Fresenius Kabi USA, LLC

Recalled Item: Ketorolac Tromethamine Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Presence of Particulate Matter - found in reserve sample vials at the firm.

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 22, 2020· Strides Pharma Inc.

Recalled Item: NDC 64380-721-06 TACROLIMUS CAPSULES Recalled by Strides Pharma Inc. Due to...

The Issue: Failed Moisture Limits

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

Class III — Low RiskOngoing
Refund
DrugDecember 22, 2020· Edge Pharma, LLC

Recalled Item: Epinephrine/Lidocaine HCl Recalled by Edge Pharma, LLC Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 22, 2020· EOS Imaging

Recalled Item: The EOSedge system may acquire two simultaneous orthogonal planar images...

The Issue: Inadequate images resizing and 2D measurement errors may occur when biplanar...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2020· Abbott Point Of Care Inc.

Recalled Item: Abbott i-STAT EG7+ cartridge-IVD. Intended for the quantitative measurement...

The Issue: Ionized calcium test on some i-STAT CG8+ and EG7+ cartridges may exhibit...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2020· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Wako HDL-C/LDL-C Calibrator - Product Usage: designed to be used Recalled by...

The Issue: FUJIFILM has become aware that incorrect concentration values were printed...

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

Class III — Low RiskOngoing
Medical DeviceDecember 22, 2020· Abbott Point Of Care Inc.

Recalled Item: Abbott i-STAT CG8+ cartridges - IVD Intended for quantitative measurement...

The Issue: Ionized calcium test on some i-STAT CG8+ and EG7+ cartridges may exhibit...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2020· Smiths Medical ASD Inc.

Recalled Item: Portex Acapella DH Vibratory PEP Device - Product Usage: a Recalled by...

The Issue: Shipping box may contain wrong model.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2020· Getinge Group Logistics America, LLC

Recalled Item: Getinge CM320 Series Washer Disinfector - Product Usage: A multi Recalled by...

The Issue: The potential that the plastic inlet hose connections may deform or break as...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2020· Nihon Kohden America Inc

Recalled Item: PSG-1100 Sleep Diagnostic System. Sample product label: JB-110A SERIAL No....

The Issue: Medical device non-conformance to electrical safety standard (IEC 60601-1).

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2020· Baxter Healthcare Corporation

Recalled Item: Baxter ONE-LINK Non-DEHP Y-Type Microbore Catheter Extension Set Recalled by...

The Issue: There were customer reports of separation between the tubing and Male Luer...

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

Class II — Potential Health HazardOngoing
DrugDecember 21, 2020· Merck Sharp & Dohme

Recalled Item: Zerbaxa (ceftolozane and tazobactam) 1.5g per vial for injection Recalled by...

The Issue: Lack of assurance of sterility: The results of sterility tests of seven...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 18, 2020· KVK-Tech, Inc.

Recalled Item: Benzhydrocodone and Acetaminophen Tablets Recalled by KVK-Tech, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications; out of specification results...

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 18, 2020· Ansh Labs, LLC

Recalled Item: AnshLabs - SARS-CoV2 IgM ELISA (u-Capture) Recalled by Ansh Labs, LLC Due to...

The Issue: Labeling update; To reduce the risk of false positive/false negative results...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2020· Topcon Medical Systems, Inc.

Recalled Item: Harmony System (aka Harmony RS)/ Medical Device Data System Recalled by...

The Issue: Harmony RS integrations with Topcon equipment, TRC NW-400 and the Signal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS Icono biplane Model:11327600 ARTIS Icono floor system Model: 11327700...

The Issue: Misleading error messages and a gap in the Operator Manual which affects...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2020· Alung Technologies Inc

Recalled Item: ALung Technologies Hemolung Respiratory Assist System (RAS) with CME...

The Issue: CME America BodyGuard 323 Infusion Pumps (recalled by manufacturer) is a...

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

Class II — Potential Health HazardOngoing