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Use caution Medical device recall · FDA · Published July 21, 2021

MPR Slotted Mallet Recall: Risk of Head Separating from Handle

Implant Resource Inc recalls MPR Slotted Mallets with potential head separation from handle and unexpected deformations. Affected units have model MPR-1120-1000 and lot numbers starting 200911-1-1. Contact 800.524.5194 for details.

🇺🇸 FDA recall #Z-0122-2022Medical deviceMPR ›
Take action

Contact the company

Official pagewww.m-p-r.com
Recalling firmImplant Resource Inc917 Lone Oak Rd Ste 1000 · Eagan, MN 55121-2266
✎ GovInfoNow plain-language explainer

Implant Resource Inc recalls MPR Slotted Mallets because the mallet head can separate from the handle during use, and the striking surface may deform unexpectedly. This could cause injury if the mallet becomes unstable or breaks during impact. Read more at govinfonow.com/recall/62174-mpr-slotted-mallet-recall-risk-of-head-separating-from-handle.

Source Summary by GovInfoNow · govinfonow.com/recall/62174-mpr-slotted-mallet-recall-risk-of-head-separating-from-handle · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0122-2022

Cite this page

“MPR Slotted Mallet Recall: Risk of Head Separating from Handle.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/62174-mpr-slotted-mallet-recall-risk-of-head-separating-from-handle. Based on FDA recall #Z-0122-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0122-2022%22&limit=1).

Implant Resource Inc. recalled MPR Slotted Mallets due to potential separation of the mallet head from the handle and unexpected surface deformations, according to the FDA. The agency announced the voluntary Class II recall on July 21, 2021.

How to tell if you have it

  • Brand: MPR
  • Product: MPR Slotted Mallet
  • Labeling: Medical Products Resource 800.524.5194 www.m-p-r.com
  • Model Number: MPR-1120-1000
  • Lot Number: 200911-1-1
  • UPC: 00840001405868

The hazard

The recall cites a potential for the mallet head to become separated from the handle. There are also significant deformations on the striking surface that were not expected, according to the FDA.

Context

GovInfoNow's records show other recent recalls of similar products include Merit Medical Custom Procedure Kit Recall (2025-12-04), Merit Medical Custom Manifold Kit Recall (2025-12-04), and Medicrea IB3D PL Instruments Set Recall (2025-10-29).

How to tell if you have this one

Check for the model number MPR-1120-1000 on the mallet and lot numbers starting with 200911-1-1. The labeling includes the phone number 800.524.5194 and website www.m-p-r.com.

  • Brand
    MPR
  • Product
    MPR Slotted Mallet, labeling etched onto devices as follows: Medical Products Resource 800.524.5194 www.m-p-r.com
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check for Model Number

    Look for the model number MPR-1120-1000 on the mallet and lot numbers starting with 200911-1-1.

  2. Contact Manufacturer

    Call 800.524.5194 or visit www.m-p-r.com for recall details and next steps.

Where it went and when

Where it was distributed

Distributed in Florida and New Hampshire.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: yesNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: yesFL

FDA distribution: “US distribution to Florida and New Hampshire” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Florida, New Hampshire.

Recall timeline

FDA published this recall 3 months after the firm started it.

1. Firm started the recall: Jul 21, 202112. FDA classified it Class II: Oct 15, 202123. Published in FDA’s Enforcement Report: Oct 27, 202132021
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

Take action

Contact MPR

We’ve drafted a message you can send MPR to request your refund or repair — edit it as you like.

Subject: Recall Z-0122-2022 — MPR Slotted Mallet Recall: Risk of Head Separating from Handle

Hello,

I own a MPR Slotted Mallet Recall: Risk of Head Separating from Handle that is covered by recall Z-0122-2022 from MPR.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-0122-2022 (July 21, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0122-2022 to see it in context.
  • Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA