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. 2,903 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,903 in last 12 months

Showing 101120 of 52,535 recalls

Medical DeviceJanuary 23, 2026· Datascope Corp.

Recalled Item: CS300 IABP. Software Version CS300 IABP C.01. Recalled by Datascope Corp....

The Issue: The firm has identified that the battery runtime and cycle specifications...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2026· Physio-Control, Inc.

Recalled Item: PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog...

The Issue: Due to pediatric defibrillator electrode delamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2026· Agiliti Health - Ellis

Recalled Item: Adapt Pump Recalled by Agiliti Health - Ellis Due to Agiliti identified an...

The Issue: Agiliti identified an issue where the Adapt Pump (61600200-Adapt Pump)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2026· Auris Health, Inc

Recalled Item: MONARCH Platform Recalled by Auris Health, Inc Due to Device for...

The Issue: Device for bronchoscopic visualization, patient airway access has software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2026· Stryker Corporation

Recalled Item: MOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer (8cm...

The Issue: Due to a need to update the product labeling (Instructions for Use IFU) as a...

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

Class II — Potential Health HazardOngoing
DrugJanuary 21, 2026· Unichem Pharmaceuticals USA Inc.

Recalled Item: Bisoprolol Fumarate and Hydrochlorothiazide tablets Recalled by Unichem...

The Issue: cGMP Deviations: recall due to not meeting the N-Nitroso Bisoprolol impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 21, 2026· Unichem Pharmaceuticals USA Inc.

Recalled Item: Doxazosin Tablets Recalled by Unichem Pharmaceuticals USA Inc. Due to...

The Issue: Tablets/Capsules Imprinted with Wrong ID

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

Class III — Low RiskOngoing
Refund
DrugJanuary 20, 2026· ACME UNITED CORPORATION

Recalled Item: Dynarex Recalled by ACME UNITED CORPORATION Due to CGMP Deviations

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
DrugJanuary 20, 2026· ACME UNITED CORPORATION

Recalled Item: Med Nap BZK Antiseptic Towelettes (Benzalkonium Chloride 0.13%) Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 PAK Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 PAK Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
DrugJanuary 20, 2026· ACME UNITED CORPORATION

Recalled Item: Children's Healthcare of Atlanta Recalled by ACME UNITED CORPORATION Due to...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 20, 2026· ACME UNITED CORPORATION

Recalled Item: 1) BZK Antiseptic Towelettes (Benzalkonium Chloride 0.13%) 5"x7" Piedmont...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund