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. 2,825 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,825 in last 12 months

Showing 1028110300 of 52,535 recalls

Medical DeviceMarch 8, 2023· NeuroLogica Corporation

Recalled Item: Samsung GM85 Digital X-ray Imaging System-A Digital Diagnostic Mobile X-ray...

The Issue: Issue related to the operation of the arm latch within the column that...

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

Class II — Potential Health HazardOngoing
FoodMarch 7, 2023· Natural Solutions Foundation

Recalled Item: Dr. Rima Recommends The Silver Solution Immune System Support Dietary...

The Issue: Product labeled and intended to mitigate, prevent, or treat COVID-19

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 7, 2023· Compass Health Brands (Corporate Office)

Recalled Item: REX (Recovery Exercise X-Trainer) Pressure Therapy System- USER Manual....

The Issue: Error in the Introduction section of the user manual that indicates the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2023· Philips North America Llc

Recalled Item: EARLYVUE VS30 VITAL SIGNS MONITOR Software Version A.00.02 and A.00.01...

The Issue: EarlyVue VS30 Vital Signs Monitor and EarlyVue VS30 Vitals monitor Missing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2023· Philips North America Llc

Recalled Item: EarlyVue VS30 Vitals monitor with Software Versions A.00.02 and A.00.01...

The Issue: EarlyVue VS30 Vital Signs Monitor and EarlyVue VS30 Vitals monitor Missing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2023· Maquet Cardiovascular, LLC

Recalled Item: VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System Recalled by Maquet...

The Issue: Some batches of product were not sterilized to their minimum sterilization...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2023· Maquet Cardiovascular, LLC

Recalled Item: VASOVIEW HEMOPRO Recalled by Maquet Cardiovascular, LLC Due to Some batches...

The Issue: Some batches of product were not sterilized to their minimum sterilization...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2023· Maquet Cardiovascular, LLC

Recalled Item: VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System Recalled by Maquet...

The Issue: Some batches of product were not sterilized to their minimum sterilization...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2023· Philips North America

Recalled Item: ProxiDiagnost N90 R.1.0 Recalled by Philips North America Due to Philips has...

The Issue: Philips has identified a compliance issue where ProxiDiagnost N90 R.1.0,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2023· Philips North America

Recalled Item: CombiDiagnost R90 R.1.0 Recalled by Philips North America Due to Philips has...

The Issue: Philips has identified a compliance issue where ProxiDiagnost N90 R.1.0,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2023· Philips North America

Recalled Item: CombiDiagnost R90 R1.1 Recalled by Philips North America Due to Philips has...

The Issue: Philips has identified a compliance issue where ProxiDiagnost N90 R.1.0,...

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

Class II — Potential Health HazardOngoing
DrugMarch 2, 2023· Endo Pharmaceuticals, Inc.

Recalled Item: Calcitonin Salmon Nasal Spray Recalled by Endo Pharmaceuticals, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications and Subpotent Drug: High Out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 2, 2023· Breckenridge Pharmaceutical, Inc

Recalled Item: Alprazolam Tablets Recalled by Breckenridge Pharmaceutical, Inc Due to CGMP...

The Issue: CGMP Deviations: Potential risk of Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 2, 2023· Breckenridge Pharmaceutical, Inc

Recalled Item: Alprazolam Tablets Recalled by Breckenridge Pharmaceutical, Inc Due to CGMP...

The Issue: CGMP Deviations: Potential risk of Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 2, 2023· Breckenridge Pharmaceutical, Inc

Recalled Item: Alprazolam Tablets Recalled by Breckenridge Pharmaceutical, Inc Due to CGMP...

The Issue: CGMP Deviations: Potential risk of Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 2, 2023· Breckenridge Pharmaceutical, Inc

Recalled Item: Alprazolam Tablets Recalled by Breckenridge Pharmaceutical, Inc Due to CGMP...

The Issue: CGMP Deviations: Potential risk of Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 2, 2023· Breckenridge Pharmaceutical, Inc

Recalled Item: Clobazam Tablets Recalled by Breckenridge Pharmaceutical, Inc Due to CGMP...

The Issue: CGMP Deviations: Potential risk of Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 2, 2023· Breckenridge Pharmaceutical, Inc

Recalled Item: Clobazam Tablets Recalled by Breckenridge Pharmaceutical, Inc Due to CGMP...

The Issue: CGMP Deviations: Potential risk of Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 2, 2023· Stryker Corporation

Recalled Item: SafeLight Fiber Optic Cable: Clear Recalled by Stryker Corporation Due to...

The Issue: Fiber optic cables assembled with not enough epoxy on the proximal end,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion CirClamp with 1.3cm Bell & Insert Reprocessed Recalled by MEDLINE...

The Issue: The CirClamp subassembly found in the kit was the incorrect size.

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

Class II — Potential Health HazardOngoing