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. 997 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
997 in last 12 months

Showing 17521–17540 of 48,330 recalls

Medical DeviceAugust 31, 2020· ICU Medical, Inc.

Recalled Item: Appx 1.7 ml Bag Spike w/Integrated Clave Recalled by ICU Medical, Inc. Due...

The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· ICU Medical, Inc.

Recalled Item: 26 IN(66 cm) APPX 3.4ml Recalled by ICU Medical, Inc. Due to Potential for...

The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· ICU Medical, Inc.

Recalled Item: Spiros CLOSED MALE LUER w/RED CAP Recalled by ICU Medical, Inc. Due to...

The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus CHF-CB30S Choledoscope Intended Use: The device was designed to...

The Issue: The CHF-CB30S Device did not have a 510(k) clearance. Additionally, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· Vascular Solutions, Inc.

Recalled Item: Langston Dual Lumen Catheter Recalled by Vascular Solutions, Inc. Due to The...

The Issue: The inner lumen of the Langston catheter may separate from the hub during...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 31, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Medical Systems Corporation (OMSC) Evis Exera II Bronchovideoscope...

The Issue: The BF-Q180 bronchoscope is being recalled because it does not have a 510(k)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· Vascular Solutions, Inc.

Recalled Item: Langston Dual Lumen Catheter. Recalled by Vascular Solutions, Inc. Due to...

The Issue: The inner lumen of the Langston catheter may separate from the hub during...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 31, 2020· ICU Medical, Inc.

Recalled Item: 5 IN (13 cm) Appx 1.5 ml Recalled by ICU Medical, Inc. Due to Potential for...

The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· Encore Medical, LP

Recalled Item: AltiVate Reverse Small Socket Insert Recalled by Encore Medical, LP Due to...

The Issue: Product mislabeled. Use may result in a delay in surgery, stopping of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx 5.5 mL 20 Drop Admin Set w/Integrated Clave Drip Chamber...

The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx 3.3 ml Recalled by ICU Medical, Inc. Due to Potential for...

The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2020· Greiner Bio-One North America, Inc.

Recalled Item: VACUETTE TUBE 5 mL CAT Serum Separator Clot Activator Recalled by Greiner...

The Issue: Blood collection tubes experienced an issue with separation and clotting

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2020· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens epoc BGEM Test Card-In vitro diagnostic device for the Recalled by...

The Issue: Sporadically inconsistent discrepant (low bias) glucose results on card lot...

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

Class II — Potential Health HazardOngoing
FoodAugust 28, 2020· EAGLE FAMILY FOODS GROUP LLC

Recalled Item: Nice! Organic White Cheddar Popcorn Recalled by EAGLE FAMILY FOODS GROUP LLC...

The Issue: Foreign material, pieces of glass may be in the product

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 28, 2020· EAGLE FAMILY FOODS GROUP LLC

Recalled Item: 365 Whole Foods Market Organic Reduced fat &Sodium Popcorn Recalled by EAGLE...

The Issue: Foreign material, pieces of glass may be in the product

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 28, 2020· EAGLE FAMILY FOODS GROUP LLC

Recalled Item: 365 Everyday Value Organic Classic Salted Popcorn Recalled by EAGLE FAMILY...

The Issue: Foreign material, pieces of glass may be in the product

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 28, 2020· EAGLE FAMILY FOODS GROUP LLC

Recalled Item: Cretors Organic Extra Virgin Olive Oil Popcorn Recalled by EAGLE FAMILY...

The Issue: Foreign material, pieces of glass may be in the product

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 28, 2020· EAGLE FAMILY FOODS GROUP LLC

Recalled Item: 365 Whole Foods Market Organic White Cheddar Popcorn Recalled by EAGLE...

The Issue: Foreign material, pieces of glass may be in the product

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 28, 2020· EAGLE FAMILY FOODS GROUP LLC

Recalled Item: Nature's Promise Organic Lightly Salted Popcorn Recalled by EAGLE FAMILY...

The Issue: Foreign material, pieces of glass may be in the product

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 27, 2020· Treehouse Foods

Recalled Item: Signature Select Chewy Granola Bars Recalled by Treehouse Foods Due to...

The Issue: Product may contain undeclared peanut butter.

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

Class I — Serious Health HazardOngoing
Refund