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. 2,674 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,674 in last 12 months

Showing 2498125000 of 52,535 recalls

Medical DeviceJanuary 9, 2019· Philips North America, LLC

Recalled Item: PageWriter TC20 Recalled by Philips North America, LLC Due to Philips...

The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Philips North America, LLC

Recalled Item: PageWriter TC30 Recalled by Philips North America, LLC Due to Philips...

The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Philips North America, LLC

Recalled Item: PageWriter TC30 w/o trolley Government Bundle Recalled by Philips North...

The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Philips North America, LLC

Recalled Item: PageWriter TC30 w/ trolley Government Bundle Recalled by Philips North...

The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Philips North America, LLC

Recalled Item: PageWriter TC70 w/trolley Government Bundle Recalled by Philips North...

The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Philips North America, LLC

Recalled Item: PageWriter TC70 w/o trolley Government Bundle Recalled by Philips North...

The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Philips North America, LLC

Recalled Item: PageWriter TC50 Government Bundle Recalled by Philips North America, LLC Due...

The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...

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

Class II — Potential Health HazardOngoing
FoodJanuary 8, 2019· Winter Gardens Quality Foods, Inc.

Recalled Item: Chips & Chocolate Recalled by Winter Gardens Quality Foods, Inc. Due to...

The Issue: Products potentially contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 7, 2019· Acuity Surgical Devices, LLC

Recalled Item: A LINK Z INTERVERTEBRAL BODY FUSION DEVICE Product Description: A Recalled...

The Issue: Due to a manufacturing process issue, it allowed vertebral body bone screws...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2019· Acuity Surgical Devices, LLC

Recalled Item: A LINK Z INTERVERTEBRAL BODY FUSION DEVICE Product Description: A Recalled...

The Issue: Due to a manufacturing process issue, it allowed vertebral body bone screws...

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

Class II — Potential Health HazardOngoing
FoodJanuary 4, 2019· Ardent Mills, LLC

Recalled Item: MEMBERS MARK SELF RISE FLR 25LB Recalled by Ardent Mills, LLC Due to...

The Issue: Ardent Mills is voluntarily recalling certain lots of Self-Rising Flour...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 4, 2019· Ardent Mills, LLC

Recalled Item: WESTCREEK H&R SELF RISE AP FLR 25LB and 50LB Recalled by Ardent Mills, LLC...

The Issue: Ardent Mills is voluntarily recalling certain lots of Self-Rising Flour...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 4, 2019· Ardent Mills, LLC

Recalled Item: HILLTOP HEARTH SELF RISE FLR 25LB and 50LB Recalled by Ardent Mills, LLC Due...

The Issue: Ardent Mills is voluntarily recalling certain lots of Self-Rising Flour...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 4, 2019· Ardent Mills, LLC

Recalled Item: ARDENT H&R SR FLR Recalled by Ardent Mills, LLC Due to Potential Salmonella...

The Issue: Ardent Mills is voluntarily recalling certain lots of Self-Rising Flour...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Universa Firm Ureteral Stent Recalled by Cook Inc. Due to The wire guide may...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: PTFE Wire Guide Recalled by Cook Inc. Due to The wire guide may be...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Angled Tip Ureteral Catheter Set with Bentson PTFE Wire Guide Recalled by...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Bander Ureteral Diversion Open-End Stent Set Recalled by Cook Inc. Due to...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Urethral Dilation Balloon Catheter with Open Tip Recalled by Cook Inc. Due...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: C-Flex Double Pigtail Ureteral Stent Set Recalled by Cook Inc. Due to The...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing