Product Recalls in Maryland

Product recalls affecting Maryland — including food, drugs, consumer products, medical devices, and vehicles distributed to Maryland. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,063 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
1,063 in last 12 months

Showing 17141–17160 of 52,535 recalls

DrugMarch 29, 2021· Spartan Chemical Co Inc

Recalled Item: Lite'n Foamy E2 Sanitizing Handwash (Benzalkonium Chloride Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 29, 2021· Spartan Chemical Co Inc

Recalled Item: Lite'n Foamy Healthcare Personnel Handwash (Chloroxylenol Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 29, 2021· Nuri Trading LLC

Recalled Item: Thumbs Up 7 Black 25K capsule Recalled by Nuri Trading LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: Product found to be tainted with...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 29, 2021· Spartan Chemical Co Inc

Recalled Item: Lite'n Foamy Eucalyptus Mint Sanitizing Handwash (Benzalkonium Chloride...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 29, 2021· Spartan Chemical Co Inc

Recalled Item: Lite'n Foamy Lemon Blossom Hand Sanitizer (benzalkonium chloride 0.1%)...

The Issue: Microbial Contamination of Non-Sterile Products; lot tested positive for...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 29, 2021· Nuri Trading LLC

Recalled Item: 69MODE Blue 69 capsule Recalled by Nuri Trading LLC Due to Undeclared Tadalafil

The Issue: Marketed Without An Approved NDA/ANDA: Product found to be tainted with...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 26, 2021· Lupin Pharmaceuticals Inc.

Recalled Item: Cefprozil for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...

The Issue: Superpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 26, 2021· Antoto-K

Recalled Item: Thumbs Up 7 Red 70K Recalled by Antoto-K Due to Marketed without Approved...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 26, 2021· Radiometer Medical ApS

Recalled Item: PIC070 Arterial Blood Sampler PICO70 - Product Usage: Preheparinized...

The Issue: Radiometer has become aware of an issue with PICO70 Arterial Blood Sampler....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2021· Nextremity Solutions

Recalled Item: InCore Lapidus Disposable Kit 28mm Right Recalled by Nextremity Solutions...

The Issue: Product could potentially contain an undersized inner diameter of the 40mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2021· Nextremity Solutions

Recalled Item: InCore Lapidus Disposable Kit 28mm Left Recalled by Nextremity Solutions Due...

The Issue: Product could potentially contain an undersized inner diameter of the 40mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2021· Ortho-Clinical Diagnostics, INc.

Recalled Item: VITROS¿ Black Slides CATALOG #: J02316 - Product Usage: Recalled by...

The Issue: Delayed results. Ortho confirmed that two lots of VITROS Black Slides are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee ceiling-interventional Fluoroscopic X-Ray System Model Number:...

The Issue: Some Artis zee ceiling systems show an increased abrasion of the cabling at...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2021· ROi CPS LLC

Recalled Item: Regard Dressing Change Tray Recalled by ROi CPS LLC Due to ChloraPrep...

The Issue: ChloraPrep applicators in the kit can grow organisms that can result in a...

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

Class II — Potential Health HazardOngoing
FoodMarch 26, 2021· Harris Teeter

Recalled Item: HARRIS TEETER FRESH FOODS MARKET 3 Layer COOKIES & CREME Recalled by Harris...

The Issue: The firm was notified by their contract manufacture that the product...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty Direct Access Diamond Tip Trocar Recalled by Zavation Due to...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty 10G Recalled by Zavation Due to Products distributed as sterile may...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty Recalled by Zavation Due to Products distributed as sterile may not...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: 10G SINGLE CEMENT DELIVERY KIT (5 FILLERS). For use in Recalled by Zavation...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: 10G DIRECT DOUBLE BONE ACCESS KIT. For use in Orthopedic / spinal...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing