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. 2,854 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,854 in last 12 months

Showing 1008110100 of 29,093 recalls

Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: RENOVA SPINE BONE FILLER 10G 12CM CENTIM. STERILE Recalled by BIOPSYBELL...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: 10G DIRECT WORKING CANNULA BEVEL TIP 15CM Recalled by BIOPSYBELL S.R.L. Due...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: 10G COAXIAL CANNULA WITH TUOHY CONNECTION Recalled by BIOPSYBELL S.R.L. Due...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: CEMENT MIXING SYSTEM Recalled by BIOPSYBELL S.R.L. Due to Products labeled...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: 10 GAUGE CEMENT DELIVERY CANNULA Recalled by BIOPSYBELL S.R.L. Due to...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: EASYNJECT Recalled by BIOPSYBELL S.R.L. Due to Products labeled as sterile...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: 10G DIRECT SINGLE - ACCESS Recalled by BIOPSYBELL S.R.L. Due to Products...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: 11G DIRECT SINGLE - ACCESS Recalled by BIOPSYBELL S.R.L. Due to Products...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: 11G DIRECT SINGLE - DELIVERY (4 FILLERS-4 SYRINGES) Recalled by BIOPSYBELL...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: BPB medica CEMIX Recalled by BIOPSYBELL S.R.L. Due to Products labeled as...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: 10 GAUGE DIRECT UNILATERAL STYLET(1 X DIAMOND 1 X BEVEL) Recalled by...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: 8G DIRECT WORKING CANNULA BEVEL TIP Recalled by BIOPSYBELL S.R.L. Due to...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· QURA S.R.L.

Recalled Item: Spectrum Medical Quantum Standard heat exchanger Recalled by QURA S.R.L. Due...

The Issue: Product labeled as sterile may not have been adequately sterilized. In...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· BIOPSYBELL S.R.L.

Recalled Item: BPB medica RENOVA SPINE KYPHOPLASTY WORKING CANNULA AND TROCAR TIP Recalled...

The Issue: Products labeled as sterile were distributed, but may not have been sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2021· Datascope Corp.

Recalled Item: Cardiosave Hybrid IABP - Product Usage: used to inflate and Recalled by...

The Issue: There are cybersecurity vulnerabilities in a widely used low-level TCP/IP...

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

Class III — Low RiskOngoing
Medical DeviceMarch 19, 2021· Cytocell Ltd.

Recalled Item: Chromosome X Alpha-Satellite in FITC Spectrum - Product Usage: Analyte...

The Issue: Users may observe additional locus specific signals at 9q34. The device pack...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Aesculap Implant Systems LLC

Recalled Item: Univation X System Tray Sysem knee implant devices as follows: Recalled by...

The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Aesculap Implant Systems LLC

Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL488...

The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· Aesculap Implant Systems LLC

Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL482...

The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· GE Healthcare, LLC

Recalled Item: Centricity Universal Viewer - Product Usage: intended to assist in the...

The Issue: When the Cross Enterprise Display option is enabled on the Centricity...

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

Class II — Potential Health HazardOngoing