Product Recalls in Delaware

Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,668 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,668 in last 12 months

Showing 56015620 of 27,373 recalls

Medical DeviceAugust 17, 2023· Philips North America Llc

Recalled Item: Patient Information Center iX with Software Version Number 4.x in Recalled...

The Issue: Patient Information Center (PIC iX) Release 4.x Surveillance Crash Caused by...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure pack: Presource PBDS Cat. PLMHCSBHF Recalled by Cardinal Health...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure pack: Presource PBDS Recalled by Cardinal Health 200, LLC Due to...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...

The Issue: A force sensor in the occlusion detector may drift out of calibration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...

The Issue: A force sensor in the occlusion detector may drift out of calibration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...

The Issue: A force sensor in the occlusion detector may drift out of calibration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure packs: (1) Presource Pain Tray Recalled by Cardinal Health 200,...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure packs: (1) Presource PBDS Cat. PN33BPCR2 Recalled by Cardinal...

The Issue: XXX

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...

The Issue: A force sensor in the occlusion detector may drift out of calibration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure packs: (1) Presource PBDS Recalled by Cardinal Health 200, LLC Due...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Presource Fistulogram Pack Recalled by Cardinal Health 200, LLC Due to Packs...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure packs: (1) Presource PBDS Recalled by Cardinal Health 200, LLC Due...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Smiths Medical ASD Inc.

Recalled Item: Medfusion ASSEMBLY PLUNGER CASE LEFT 1/EA Recalled by Smiths Medical ASD...

The Issue: A force sensor in the occlusion detector may drift out of calibration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure packs: (1) Presource PBDS Cat. PNVMNIB21 Recalled by Cardinal...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure packs: (1) Presource Portacath Pack Recalled by Cardinal Health...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Smiths Medical ASD Inc.

Recalled Item: Medfusion PLUNGER FLOAT PLATE Recalled by Smiths Medical ASD Inc. Due to A...

The Issue: A force sensor in the occlusion detector may drift out of calibration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure packs: (1) Presource PBDS Cat. PG33BTO21 Recalled by Cardinal...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2023· Remel, Inc

Recalled Item: remel TODD HEWITT W. CNA (LIM BROTH) Recalled by Remel, Inc Due to On lot of...

The Issue: On lot of Todd Hewitt Broth w/CNA (LIM) may exhibit no recovery of target...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2023· Microbiologics Inc

Recalled Item: KWIK-STIK Recalled by Microbiologics Inc Due to One lot of KWIK STIK ANA (3...

The Issue: One lot of KWIK STIK ANA (3 strains) QC Set is missing one of the strains,...

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

Class III — Low RiskOngoing
Medical DeviceAugust 10, 2023· Turncare, Inc

Recalled Item: Brand Name: Guardian 2 System Product Name: Guardian System 2 Recalled by...

The Issue: A software update corrected an issue where "low" and "terminal" battery...

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

Class II — Potential Health HazardOngoing