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. 2,890 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
2,890 in last 12 months

Showing 33813400 of 29,947 recalls

Medical DeviceJuly 31, 2024· Beckman Coulter Inc.

Recalled Item: IMMAGE Immunochemistry Systems IGM Immunoglobulin M Reagent IGM Recalled by...

The Issue: Firm identified two lots of reagents that are not meeting the sensitivity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ Total Bilirubin (TBIL) Flex Reagent Cartridge Recalled by...

The Issue: During manufacturing, the last three tests from the 160 test flex of lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by Siemens...

The Issue: The potential for biased quality control (QC) and patient results when using...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2024· Siemens Healthcare Diagnostics, Inc.

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

The Issue: The potential for biased quality control (QC) and patient results when using...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2024· Agfa N.V.

Recalled Item: DR 800. Digital Radiography X-ray System. Recalled by Agfa N.V. Due to...

The Issue: Potential for the front lever chain of the DR 800 table to fail.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing