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. 2,878 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
2,878 in last 12 months

Showing 59415960 of 29,947 recalls

Medical DeviceJuly 26, 2023· Zimmer, Inc.

Recalled Item: M/L Taper Hip Prosthesis Extended Offset Recalled by Zimmer, Inc. Due to The...

The Issue: The outer package labeling and product etch are for a Size 6, however, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2023· SenTec AG

Recalled Item: Membrane Changer Single-Use Recalled by SenTec AG Due to During rework of...

The Issue: During rework of components during the manufacturing process, an additional...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2023· Diversatek Healthcare

Recalled Item: ZVU Functional GI Software Recalled by Diversatek Healthcare Due to GI...

The Issue: GI Software labelled as revision 3.3.0 is incorrectly labeled and is in fact...

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

Class III — Low RiskOngoing
Medical DeviceJuly 25, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by...

The Issue: There is a potential for ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2023· Medtronic Navigation, Inc.-Littleton

Recalled Item: The O-arm O2 Imaging System is a mobile x-ray system Recalled by Medtronic...

The Issue: Ground cable installed incorrectly.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2023· Cook Vandergrift, Inc.

Recalled Item: Cook Lead Clipper- An auxiliary tool indicated for use in Recalled by Cook...

The Issue: Sterility of device may be compromised due to breach of the chevron seal of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2023· Smith & Nephew, Inc.

Recalled Item: TRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 36CM 130 DEGREE LEFT...

The Issue: A complaint was received indicating that a package contained a TRIGEN...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2023· Smith & Nephew, Inc.

Recalled Item: TRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 40CM 130 DEGREE LEFT...

The Issue: A complaint was received indicating that a package contained a TRIGEN...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2023· Ambu Inc.

Recalled Item: Ambu aView 2 A Monitor-The Ambu aView 2 Advance is Recalled by Ambu Inc. Due...

The Issue: Multiple impacts, for example from being dropped, can cause to the Ambu...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2023· Keystone Industries

Recalled Item: Keystone Bosworth Copaliner Cavity Varnish .5oz (14 ml)- Intended to...

The Issue: A bottle of Copaliner Solvent was inadvertently packaged into a box labeled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2023· Philips Medical Systems Nederland B.V.

Recalled Item: Zenition 70. The device is to be used in health Recalled by Philips Medical...

The Issue: Philips has become aware of the potential for unintended radiation exposure...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2023· Cosmedent, Inc.

Recalled Item: Cosmedent FlexiCup Composite Finishing & Polishing System Recalled by...

The Issue: Reports were received the elastomer cup material is crumbling.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2023· Aesculap Implant Systems LLC

Recalled Item: For intraventricular indications mainly used for operations within the brain...

The Issue: Trocar manufactured with the shaft too long and does not meet manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2023· Olympus Corporation of the Americas

Recalled Item: Visera Hysterovideoscope Olympus HYF Type V Recalled by Olympus Corporation...

The Issue: IFU labeling is being updated to revise EtO gas mixture and elimination of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2023· Reichert, Inc.

Recalled Item: PHOROPTOR VRX DIGITAL SYSTEM-Digital intended for the subjective Recalled by...

The Issue: Phoroptor VRx Head may detach from the bracket that connects the Phoroptor...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2023· NOXBOX LTD

Recalled Item: NOxBOXi Nitric Oxide Delivery System Recalled by NOXBOX LTD Due to...

The Issue: Replacement of the internal Sample Pump due to high failure rates.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2023· IHB OPERATIONS B.V.

Recalled Item: Freedom Boom models series: F110 Recalled by IHB OPERATIONS B.V. Due to...

The Issue: Weakened connection point on the adjustable suspension arm, potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2023· Philips Medical Systems Nederland B.V.

Recalled Item: Allura Xper series Recalled by Philips Medical Systems Nederland B.V. Due to...

The Issue: A foot switch pedal may get stuck in the active position when the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2023· Philips Medical Systems Nederland B.V.

Recalled Item: Azurion Recalled by Philips Medical Systems Nederland B.V. Due to A foot...

The Issue: A foot switch pedal may get stuck in the active position when the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2023· Philips Medical Systems Nederland B.V.

Recalled Item: MultiDiagnost-Eleva Recalled by Philips Medical Systems Nederland B.V. Due...

The Issue: A foot switch pedal may get stuck in the active position when the user...

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

Class II — Potential Health HazardOngoing