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. 2,655 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,655 in last 12 months

Showing 79617980 of 48,330 recalls

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
DrugAugust 11, 2023· Baxter Healthcare Corporation

Recalled Item: Dianeal PD-2 Peritonial Dialysis Solution with 1.5% Dextrose Recalled by...

The Issue: Lack of Assurance of Sterility: Potential presence of leaks originating from...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 11, 2023· Baxter Healthcare Corporation

Recalled Item: DIANEAL Low Calcium (2.5 mEq/L) Peritoneal Dialysis Solution 1.5% Dextrose...

The Issue: Lack of Assurance of Sterility: Potential presence of leaks originating from...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2023· Imprimis NJOF, LLC

Recalled Item: Moxifloxacin - Bromfenac Sterile Ophthalmic Solution 0.5% / 0.075% Recalled...

The Issue: Subpotent Drug; sub-potent Bromfenac levels, below the 90.0-110.0%...

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

Class III — Low RiskOngoing
Refund
DrugAugust 10, 2023· Colgate Palmolive Company

Recalled Item: hello wild strawberry fluoride toothpaste Recalled by Colgate Palmolive...

The Issue: Labeling: Label Mix-Up: Some hello wild strawberry fluoride toothpaste,...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 10, 2023· Conopco DBA Unilever

Recalled Item: Knorr Fideos con Tomate Tomato Based Pasta Soup Mix 3.5 oz Recalled by...

The Issue: Undeclared egg

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodAugust 10, 2023· Conopco DBA Unilever

Recalled Item: Knorr Letras con Tomate Tomato Based Alphabet Pasta Soup Mix Recalled by...

The Issue: Undeclared egg

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodAugust 10, 2023· Conopco DBA Unilever

Recalled Item: Knorr Estrellitas con Tomate Tomato Based Star Pasta Soup Mix Recalled by...

The Issue: Undeclared egg

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
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
Medical DeviceAugust 10, 2023· Covidien

Recalled Item: McGrath Mac 2 Recalled by Covidien Due to Laryngoscope blades may contain an...

The Issue: Laryngoscope blades may contain an ineffective application of anti-fog agent...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Covidien

Recalled Item: McGrath Mac 2 Recalled by Covidien Due to Laryngoscope blades may contain an...

The Issue: Laryngoscope blades may contain an ineffective application of anti-fog agent...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Olympus Corporation of the Americas

Recalled Item: Veran : Endobronchial Always on Track Models: INS-0392 AOTT 21ga Needle...

The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Olympus Corporation of the Americas

Recalled Item: Veran : Percutaneous Always on Track Models: INS-5040 Always-On vTrack...

The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Olympus Corporation of the Americas

Recalled Item: Veran:SPiN Thoracic Navigation System Models: SYS-4230 SPiN Thoracic...

The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Olympus Corporation of the Americas

Recalled Item: Veran : Percutaneous Models: INS-5620 SPiN Perc Biopsy Needle Guide Kit -...

The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Olympus Corporation of the Americas

Recalled Item: Veran : Endobronchial Models: INS-5500 View Optical Probe INS-5450 SPiN...

The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Olympus Corporation of the Americas

Recalled Item: Veran Endobronchial: Models: INS-5925 SPiN Access Catheter¿ 180 Degree for...

The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Bard Peripheral Vascular Inc

Recalled Item: Bard Marquee Disposable Core Biopsy Instrument Kit Recalled by Bard...

The Issue: Diameter mismatch between coaxial and biopsy needle (cutting cannula) in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Epiphany Cardio Server E3 ECG Management System Servers with Recalled...

The Issue: Epiphany, now a Baxter Healthcare company, is issuing an Urgent Medical...

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

Class II — Potential Health HazardOngoing