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. 2,010 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,010 in last 12 months

Showing 72217240 of 52,535 recalls

Medical DeviceJanuary 9, 2024· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Abbott Rapid Dx N America LLC Reproductive Endocrinology Control Set...

The Issue: Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Dr Franz Koehler Chemie Gmbh

Recalled Item: Custodiol HTK Solution Recalled by Dr Franz Koehler Chemie Gmbh Due to...

The Issue: Potential for particles to be present in solution.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Steris Corporation Endo Cleaning Indicator VERIFY" RESITEST" Recalled by...

The Issue: Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Sulfamethoxazole with Trimethoprim 23.75/1.25 ug Recalled...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Ertapenem- 10 ug Recalled by Becton Dickinson & Co. Due to...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Ampicillin - 10 ¿g Recalled by Becton Dickinson & Co. Due...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Chloramphenicol- 30 ug Recalled by Becton Dickinson & Co....

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: Sensi Disc Amoxicillin with Clavulanic Acid 20/10 ¿g Recalled by Becton...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Cefixime - 5 ug¿ Recalled by Becton Dickinson & Co. Due to...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Cefaclor - 30 ug¿ Recalled by Becton Dickinson & Co. Due...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Ofloxacin- 5 ug Recalled by Becton Dickinson & Co. Due to...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Cefotaxime - 30 ug¿ Recalled by Becton Dickinson & Co. Due...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing