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. 1,670 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
1,670 in last 12 months

Showing 4420144220 of 48,330 recalls

DrugMay 29, 2013· Lowlite Investments, Inc. D/B/A Olympia Pharmacy

Recalled Item: Acepromazine 25 mg/ml Injection Recalled by Lowlite Investments, Inc. D/B/A...

The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 29, 2013· Lowlite Investments, Inc. D/B/A Olympia Pharmacy

Recalled Item: Glutathione 200 mg/ml Injection Recalled by Lowlite Investments, Inc. D/B/A...

The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 29, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens MEVATRON series Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: The information regarding the FILM Mode calibration may have been considered...

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

Class II — Potential Health HazardOngoing
FoodMay 29, 2013· Conagra Inc

Recalled Item: Lightlife Farmer's Market Veggie Burgers Recalled by Conagra Inc Due to The...

The Issue: The product packaging for Lighthouse Farmer's Market Veggie Burgers may...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 28, 2013· Coca-Cola Refreshments USA, Inc.

Recalled Item: MINUTE MAID STRAWBERRY PASSION Flavored Juice Beverage Recalled by Coca-Cola...

The Issue: Products with the specific Lot Code and Codes listed above are being...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 28, 2013· Coca-Cola Refreshments USA, Inc.

Recalled Item: MINUTE MAID APPLE JUICE Recalled by Coca-Cola USA, Inc. Due to Products with...

The Issue: Products with the specific Lot Code and Codes listed above are being...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 28, 2013· Coca-Cola Refreshments USA, Inc.

Recalled Item: MINUTE MAID Mixed Berry Juice Recalled by Coca-Cola USA, Inc. Due to...

The Issue: Products with the specific Lot Code and Codes listed above are being...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 28, 2013· Coca-Cola Refreshments USA, Inc.

Recalled Item: MINUTE MAID ORANGE JUICE Recalled by Coca-Cola USA, Inc. Due to Products...

The Issue: Products with the specific Lot Code and Codes listed above are being...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 28, 2013· Coca-Cola Refreshments USA, Inc.

Recalled Item: MINUTE MAID CRANBERRY APPLE RASPBERRY Flavored Juice Beverage Recalled by...

The Issue: Products with the specific Lot Code and Codes listed above are being...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 28, 2013· Boston Scientific Corporation

Recalled Item: Alair Bronchial Thermoplasty Catheter Recalled by Boston Scientific...

The Issue: Boston Scientific has discovered an inconsistent "Use By" expiration date on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Boston Scientific Corporation

Recalled Item: NephroMax high Pressure Nephrostomy Balloon Catheter. Material...

The Issue: Incorrect sized renal sheath was packaged with the NephroMax high pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Bard Peripheral Vascular Inc

Recalled Item: BARD PERIPHERAL VASCULAR VACCESS¿ PTA Balloon Dilatation Catheters Recalled...

The Issue: Bard Peripheral Vascular (BPV) has confirmed that some product code/lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· DJO, LLC

Recalled Item: VenaFlow Elite 30B-B and 30BI-B Product Usage: The VenaFlow Elite Recalled...

The Issue: DJO, LLC has recently identified a product safety issue with the battery...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Medtronic Sofamor Danek USA Inc

Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...

The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Beckman Coulter Inc.

Recalled Item: SYNCHRON System(s) Lactate (LACT) Reagent. Product Usage: Lactate (LACT)...

The Issue: Beckman Coulter has confirmed customer reports of LACT Lot M210077 failing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Medtronic Sofamor Danek USA Inc

Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...

The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Medtronic Sofamor Danek USA Inc

Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...

The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Medtronic Sofamor Danek USA Inc

Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...

The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Medtronic Sofamor Danek USA Inc

Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...

The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Medtronic Sofamor Danek USA Inc

Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...

The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...

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

Class II — Potential Health HazardOngoing