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. 2,583 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,583 in last 12 months

Showing 5006150080 of 52,535 recalls

DrugNovember 21, 2012· Hill Dermaceuticals, Inc.

Recalled Item: Derma-Smoothe/FS (fluocinolone acetonide) 0.01% Topical Oil(SCALP OIL)...

The Issue: Subpotent; 22 month stability timepoint

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

Class III — Low RiskOngoing
Refund
DrugNovember 21, 2012· Hill Dermaceuticals, Inc.

Recalled Item: Derma-Smoothe/FS (fluocinolone acetonide) Recalled by Hill Dermaceuticals,...

The Issue: Subpotent; 12 month stability timepoint

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

Class III — Low RiskOngoing
Refund
DrugNovember 21, 2012· Bracco Diagnostic Inc

Recalled Item: Isovue -370 (Iopamidol) Injection 76% Recalled by Bracco Diagnostic Inc Due...

The Issue: Presence of Particulate Matter; fibers identified as cellulose and polyvinyl

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 21, 2012· Bracco Diagnostic Inc

Recalled Item: Isovue -300 (Iopamidol) Injection 61% Prefilled Recalled by Bracco...

The Issue: Presence of Particulate Matter; fibers identified as cellulose and polyvinyl

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 21, 2012· Hospira, Inc.

Recalled Item: Nalbuphine HCl Injection Recalled by Hospira, Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Complains of a loose crimp applied to the...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 21, 2012· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Fluorouracil Topical Cream USP Recalled by Taro Pharmaceuticals U.S.A., Inc....

The Issue: Product Lacks Stability: Out-of-specification (OOS) results were observed...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 21, 2012· Remel Inc

Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...

The Issue: Boxes labeled as CIP5 may contain cartridges of AMP5.

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Positive and Negative Control Strips for Urine Chemistry...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Combo Pak (Distributed OUS only) Catalog Number: 1364M...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Positive and Negative Control Strips for Urine Chemistry...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Combo Pak (Distributed OUS only) Catalog Number: 1364N...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Combo Pak Catalog Number: 1364 Chek-Stix¿ Positive and...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Combo Pak (Distributed OUS) Catalog Number: 1364E...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens CLINITEK Atlas Positive and Negative Control Strips for Urine...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
FoodNovember 20, 2012· Whole Foods Market

Recalled Item: 365 Organic Orzo Recalled by Whole Foods Market Due to This product (one...

The Issue: This product (one specific lot code) was being held at the manufacturers'...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 20, 2012· GE Healthcare It

Recalled Item: The Centricity Laboratory System is intended to be an information Recalled...

The Issue: GE Healthcare is aware of a potential safety issue associated with the use...

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

Class III — Low RiskOngoing
Medical DeviceNovember 20, 2012· ConMed Corporation

Recalled Item: WANG Transbronchial Aspiration Needles Cat. No. MW-221 Recalled by ConMed...

The Issue: ConMed received complaints from a user facility reporting that the WANG...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2012· ConMed Corporation

Recalled Item: WANG Transbronchial Aspiration Needles Cat. No. MW-322 Recalled by ConMed...

The Issue: ConMed received complaints from a user facility reporting that the WANG...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2012· ConMed Corporation

Recalled Item: WANG Transbronchial Aspiration Needles Cat. No. SW-121 Recalled by ConMed...

The Issue: ConMed received complaints from a user facility reporting that the WANG...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2012· ConMed Corporation

Recalled Item: WANG Transbronchial Aspiration Needles Cat. No. MW-222 Recalled by ConMed...

The Issue: ConMed received complaints from a user facility reporting that the WANG...

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

Class II — Potential Health HazardOngoing