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. 2,906 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
2,906 in last 12 months

Showing 28012820 of 29,947 recalls

Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp EX Short...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Atellica CH Reaction Ring Cuvette Segment-has cuvettes that contain...

The Issue: A manufacturing defect causes Atellica CH Reaction Ring Cuvette Segments...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2024· Biomet, Inc.

Recalled Item: JuggerLoc/ToggleLoc 2.9mm Drill Guide Recalled by Biomet, Inc. Due to Firm...

The Issue: Firm received complaints reporting that guides were warped when pulled out...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Karl Storz Endoscopy

Recalled Item: Irrigation Tubing for KARL STORZ Endomat Select UP210 Recalled by Karl Storz...

The Issue: Due to improper labeling of products. An intended use on the label has not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Iris Scissors Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Tip protector may fall off within the packaging, resulting in compromised...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2024· HUMAN MED AG

Recalled Item: human med Biofill Infiltration Cannula Recalled by HUMAN MED AG Due to The...

The Issue: The cannula tubes do not comply with the specification. The water jet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2024· LivaNova Deutschland GmbH

Recalled Item: Essenz HLM (Heart-Lung Machine) Recalled by LivaNova Deutschland GmbH Due to...

The Issue: Heart-Lung Machine GUI touchscreen may go dark for 10-15 seconds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2024· CORNEAT VISION, LTD.

Recalled Item: CorNeat EverPatch Recalled by CORNEAT VISION, LTD. Due to Retroactive; Due...

The Issue: Retroactive; Due to complaints, labeling correction for permanent...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE procedure kits labeled as follows: 1) COMBINED SPINAL AND EPIDURAL...

The Issue: The connectors may not allow catheters to be inserted as intended if the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2024· IDS LTD

Recalled Item: Smaxel Fractional CO2 Laser Recalled by IDS LTD Due to The Smaxel Fractional...

The Issue: The Smaxel Fractional CO2 Laser does not include a Certification label, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE procedure kits labeled as follows: 1) CONT EPI 20G W/HUSTEAD...

The Issue: The connectors may not allow catheters to be inserted as intended if the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE procedure kits labeled as follows: 1) 20G EPI CATH SINGLE STERILE...

The Issue: The connectors may not allow catheters to be inserted as intended if the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE procedure kits labeled as follows: 1) ECHOSTIM BLOCK SET Recalled by...

The Issue: The connectors may not allow catheters to be inserted as intended if the...

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

Class II — Potential Health HazardOngoing