Product Recalls in Massachusetts

Product recalls affecting Massachusetts — including food, drugs, consumer products, medical devices, and vehicles distributed to Massachusetts. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,012 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
1,012 in last 12 months

Showing 37201–37220 of 52,647 recalls

Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
DrugJanuary 21, 2016· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corp. Due...

The Issue: Lack of Assurance of Sterility: potential for leaking containers which lacks...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 21, 2016· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corp. Due...

The Issue: Presence of Particulate Matter: identified as cardboard.

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 21, 2016· Baxter Healthcare Corp.

Recalled Item: Metronidazole Injection USP Recalled by Baxter Healthcare Corp. Due to...

The Issue: Presence of Particulate Matter: identified as a cloth fiber.

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 21, 2016· Baxter Healthcare Corp.

Recalled Item: CLINIMIX E 5/15 sulfite-free (5% Amino Acid with Electrolytes in Recalled by...

The Issue: Presence of Particulate Matter: identified as dried skin.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 20, 2016· Ouhlala Gourmet Llc

Recalled Item: Fruit Tartlets Recalled by Ouhlala Gourmet Llc Due to Undeclared Milk

The Issue: Products contain undeclared milk on finished product labeling

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

Class II — Potential Health HazardOngoing
Refund